For typeset documentation, examples of use, and design philosophy please go to my blog.

To facilitate the multiple phases of the dazzler assembler, we organize all the read data into what is effectively a "database" of the reads and their meta-information. The design goals for this data base are as follows:

1. The database stores the source Pacbio read information in such a way that it can recreate the original input data, thus permitting a user to remove the (effectively redundant) source files. This avoids duplicating the same data, once in the source file and once in the database.

2. The data base can be built up incrementally, that is new sequence data can be added to the data base over time.

3. The data base flexibly allows one to store any meta-data desired for reads. This is accomplished with the concept of tracks that implementors can add as they need them.

4. The data is held in a compressed form equivalent to the .dexta and .dexqv/.dexar files of the data extraction module.

5. Quiver or Arrow information can be added separately from the sequence information and later on if desired, but a database can only hold either Quiver or Arrow information, but not both. The Arrow or Quiver information can be removed from the database at any time leaving a database just containing sequence information.

6. To facilitate job parallel, cluster operation of the phases of our assembler, the data base has a concept of a current partitioning in which all the reads that are over a given length and optionally unique to a well, are divided up into blocks containing roughly a given number of bases, except possibly the last block which may have a short count. Often programs con be run on blocks or pairs of blocks and each such job is reasonably well balanced as the blocks are all the same size. One must be careful about changing the partition during an assembly as doing so can void the structural validity of any interim block-based results.

A DB con contain the information needed by Quiver, or by Arrow, or neither, but not both. A DB containing neither Quiver or Arrow information is termed a Sequence-DB (S-DB). A DB with Quiver information is a Quiver-DB (Q-DB) and a DB with Arrow information is an Arrow-DB (A-DB). All commands are aware of the state of a DB and respond to options according to their type.

A Dazzler DB consists of one named, visible file, e.g. FOO.db, and several invisible secondary files encoding various elements of the DB. The secondary files are "invisible" to the UNIX OS in the sense that they begin with a "." and hence are not listed by "ls" unless one specifies the -a flag. We chose to do this so that when a user lists the contents of a directory they just see a single name, e.g. FOO.db, that is used to refer to the DB in commands. The files associated with a database named, say FOO, are as follows:

• "FOO.db": a text file containing

  1. the list of input files added to the database so far, and
  2. how to partition the database into blocks (if the partition parameters have been set).

• ".FOO.idx": a binary "index" of all the meta-data about each read allowing, for example, one to randomly access a read's sequence (in the store ".FOO.bps"). It is 28N + 88 bytes in size where N is the number of reads in the database.

• ".FOO.bps": a binary compressed "store" of all the DNA sequences. It is M/4 bytes in size where M is the total number of base pairs in the database.

• ".FOO.qvs": a binary compressed "store" of the 5 Pacbio quality value streams for the reads. Its size is roughly 5/3M bytes depending on the compression acheived. This file only exists if Quiver information has been added to the database.

• ".FOO.arw": a binary compressed "store" of the clipped pulse width stream for the reads. Its size is roughly M/4 bytes. This file only exists if Arrow information has been added to the database.

• ".FOO.<track>.[anno,data]": a track containing customized meta-data for each read. For example, the DBdust command annotates low complexity intervals of reads and records the intervals for each read in two files .FOO.dust.anno & .FOO.dust.data. Any kind of information about a read can be recorded, such as micro-sats, repeat intervals, corrected sequence, etc. Specific tracks will be described as modules that produce them are released.

If one does not like the convention of the secondary files being invisible, then un-defining the constant HIDE_FILES in DB.h before compiling the library, creates commands that do not place a prefixing "." before secondary file names, e.g. FOO.idx instead of .FOO.idx. One then sees all the files realizing a DB when listing the contents of a directory with ls.

While a Dazzler DB holds a collection of Pacbio reads, a Dazzler map DB or DAM holds a collection of contigs from a reference genome assembly. This special type of DB has been introduced in order to facilitate the mapping of reads to an assembly and has been given the suffix .dam to distinguish it from an ordinary DB. It is structurally identical to a .db except:

• there is no concept of quality values, and hence no .FOO.qvs or .FOO.arw file.

• every .fasta scaffold (a sequence with runs of N's between contigs estimating the length of the gap) is broken into a separate contig sequence in the DB and the header for each scaffold is retained in a new .FOO.hdr file.

• the original and first and last pulse fields in the meta-data records held in .FOO.idx, hold instead the contig number and the interval of the contig within its original scaffold sequence.

A map DB can equally well be the argument of many of the commands below that operate on normal DBs. In general, a .dam can be an argument anywhere a .db can, with the exception of routines or optioned calls to routines that involve quality values, or the special routines fasta2DAM and DAM2fasta that create a DAM and reverse said, just like the pair fasta2DB and DB2fasta do for a normal DB. So in general when we refer to a database we are referring to either a DB or a DAM.

The command DBsplit sets or resets the current partition for a database which is determined by 3 parameters: (i) the total number of basepairs to place in each block, (ii) the minimum read length of reads to include within a block, and (iii) whether or not to only include the longest (-l) or median (-m) read from a given well or all reads from a well (-a) (NB: several reads of the same insert in a given well can be produced by the Pacbio instrument). Note that the length and uniqueness parameters effectively select a subset of the reads that contribute to the size of a block. We call this subset the trimmed data base. Some commands operate on the entire database, others on the trimmed database, and yet others have an option flag that permits them to operate on either at the users discretion. Therefore, one should note carefully to which version of the database a command refers to. This is especially important for any command that identifies reads by their index (ordinal position) in the database.

Once the database has been split into blocks, the commands DBshow, DBstats, and DBdust below and commands yet to come, such as the local alignment finder dalign, can take a block or blocks as arguments. On the command line this is indicated by supplying the name of the DB followed by a period and then a block number, e.g. FOO.3.db or simply FOO.3, refers to the 3'rd block of DB FOO (assuming of course it has a current partition and said partition has a 3rd block). One should note carefully that a block is a contiguous range of reads such that once it is trimmed has a given size in base pairs (as set by DBsplit). Thus like an entire database, a block can be either untrimmed or trimmed and one needs to again be careful when giving a read index to a command such as DBshow.

All programs add suffixes (e.g. .db) as needed. The commands of the database library are currently as follows:

1. fasta2DB [-v] <path:db> ( -f<file> | -i[<name>] | <input:fasta> ... )

Builds an initial data base, or adds to an existing database, either (a) the list of .fasta files following the database name argument, or (b) the list of .fasta files in <file> if the -f option is used, or (c) entries piped from the standard input if the -i option is used. If the DB is being created it is established as a Sequence-DB (S-DB) otherwise its type is unchanged. If a faux file name, <name>, follows the -i option then all the input received is considered to have come from a file by the name of <name>.fasta by DB2fasta, otherwise it will be sent to the standard output by DB2fasta. The SMRT cells in a given named input (i.e. all sources other than -i without a name) can only be added consecutively to the DB (this is checked by the command). The .fasta headers must be in the "Pacbio" format (i.e. the output of the Pacbio tools or our dextract program) and the well, pulse interval, and read quality are extracted from the header and kept with each read record. The headers may now also be those Pacbio outputs for CCS data wherein the pulse range is replaced by the string "ccs" and in which case only the well number is recorded. If the files are being added to an existing database, and the partition settings of the DB have already been set (see DBsplit below), then the partitioning of the database is updated to include the new data. A file may contain the data from multiple SMRT cells provided the reads for each SMRT cell are consecutive in the file.

2. DB2fasta [-vU] [-w<int(80)>] <path:db>

The set of .fasta files for the given DB are recreated from the DB exactly as they were input. That is, this is a perfect inversion, including the reconstitution of the proper .fasta headers. Because of this property, one can, if desired, delete the .fasta source files once they are in the DB as they can always be recreated from it. Entries imported from the standard input will be place in the faux file name given on import, or to the standard output if no name was given. By default the output sequences are in lower case and 80 chars per line. The -U option specifies upper case should be used, and the characters per line, or line width, can be set to any positive value with the -w option.

3. quiva2DB [-vl] <path:db> ( -f<file> | -i | <input:quiva> ... )

Adds .quiva streams to an existing DB "path". The DB must either be an S-DB or a Q-DB and upon completion the DB is a Q-DB. The data comes from (a) the given .quiva files on the command line, or (b) those in the file specified by the -f option, or (c) the standard input if the -i option is given. The input files can be added incrementally but must be added in the same order as the .fasta files were and have the same root names, e.g. FOO.fasta and FOO.quiva. This is enforced by the program. With the -l option set the compression scheme is a bit lossy to get more compression (see the description of dexqv in the DEXTRACTOR module here).

4. DB2quiva [-vU] <path:db>

The set of .quiva files within the given Q-DB are recreated from the DB exactly as they were input. That is, this is a perfect inversion, including the reconstitution of the proper .quiva headers. Because of this property, one can, if desired, delete the .quiva source files once they are in the DB as they can always be recreated from it. Entries imported from the standard input will be placed in the faux file name given on import, or to the standard output if no name was given. By .fastq convention each QV vector is output as a line without new-lines, and by default the Deletion Tag entry is in lower case letters. The -U option specifies upper case letters should be used instead.

5. arrow2DB [-v] <path:db> ( -f<file> | -i | <input:arrow> ... )

Adds .arrow streams to an existing DB "path". The DB must either be an S-DB or an A-DB and upon completion the DB is an A-DB. The data comes from (a) the given .arrow files on the command line, or (b) those in the file specified by the -f option, or (c) the standard input if the -i option is given. The input files can be added incrementally but must be added in the same order as the .fasta files were and have the same root names, e.g. FOO.fasta and FOO.quiva. This is enforced by the program.

6. DB2arrow [-v] [-w<int(80)>] <path:db>

The set of .arrow files within the given A-DB are recreated from the DB exactly as they were input. That is, this is a perfect inversion, including the reconstitution of the proper .arrow headers. Because of this property, one can, if desired, delete the .arrow source files once they are in the DB as they can always be recreated from it. Entries imported from the standard input will be placed in the faux file name given on import, or to the standard output if no name was given. By default the output sequences are formatted 80 chars per line, but the characters per line, or line width, can be set to any positive value with the -w option.

7. fasta2DAM [-v] <path:dam> ( -f<file> | -i[<name>] | <input:fasta> ... )

Builds an initial map DB or DAM, or adds to an existing DAM, either (a) the list of .fasta files following the database name argument, or (b) the list of .fasta files in <file> if the -f option is used, or (c) entries piped from the standard input if the -i option is used. If a faux file name, <name>, follows the -i option then all the input received is considered to have come from a file by the name of <name>.fasta by DAM2fasta, otherwise it will be sent to the standard output by DAM2fasta. Any .fasta entry that has a run of N's in it will be split into separate "contig" entries and the interval of the contig in the original entry recorded. The header for each .fasta entry is saved with the contigs created from it.

8. DAM2fasta [-vU] [-w<int(80)>] <path:dam>

The set of .fasta files for the given map DB or DAM are recreated from the DAM exactly as they were input. That is, this is a perfect inversion, including the reconstitution of the proper .fasta headers and the concatenation of contigs with the proper number of N's between them to recreate scaffolds. Entries imported from the standard input will be place in the faux file name given on import, or to the standard output if no name was given. By default the output sequences are in lower case and 80 chars per line. The -U option specifies upper case should be used, and the characters per line, or line width, can be set to any positive value with the -w option.

9. DBsplit [-aflm] [-x<int>] [-s<double(200.)>] <path:db|dam>

Divide the database <path>.db or <path>.dam conceptually into a series of blocks referable to on the command line as <path>.1, <path>.2, ... If the -x option is set then all reads less than the given length are ignored, and if the -a option is not set then secondary reads from a given well are also ignored. The remaining reads, constituting what we call the trimmed DB, are split amongst the blocks so that each block is of size -s * 1Mbp except for the last which necessarily contains a smaller residual. The default value for -s is 200Mbp because blocks of this size can be compared by our "overlapper" dalign in roughly 16Gb of memory. The blocks are very space efficient in that their sub-index of the master .idx is computed on the fly when loaded, and the .bps and .qvs files (if a .db) of base pairs and quality values, respectively, is shared with the master DB. Any relevant portions of tracks associated with the DB are also computed on the fly when loading a database block. If the -f option is set, the split is forced regardless of whether or not the DB in question has previously bin split, i.e. one is not interactively asked if they wish to proceed.

By default, the primary read for each well consists of the longest subread of the insert from the well. By setting the -m parameter, the subread of median length becomes the primary read instead. One can at any later time change this back to the default longest by splitting again with the -l parameter set. The setting of the primary reads occurs regardless of whether the -a parameter is set or not.

10. DBtrim [-af] [-x<int>] <path:db|dam>

Exactly like DBsplit except that it only resets the trimming parameters (and not the split partition itself).

11. DBdust [-b] [-w<int(64)>] [-t<double(2.)>] [-m<int(10)>] <path:db|dam>

Runs the symmetric DUST algorithm over the reads in the untrimmed DB <path>.db or <path>.dam producing a track .<path>.dust[.anno,.data] that marks all intervals of low complexity sequence, where the scan window is of size -w, the threshold for being a low-complexity interval is -t, and only low-complexity intervals of size greater than -m are recorded. If the -b option is set then the definition of low complexity takes into account the frequency of a given base. The command is incremental if given a DB to which new data has been added since it was last run on the DB, then it will extend the track to include the new reads. It is important to set this flag for genomes with a strong AT/GC bias, albeit the code is a tad slower. The dust track, if present, is understood and used by DBshow, DBstats, and dalign.

DBdust can also be run over an untriimmed DB block in which case it outputs a track encoding where the trace file names contain the block number, e.g. .FOO.3.dust.anno and .FOO.3.dust.data, given FOO.3 on the command line. We call this a block track. This permits job parallelism in block-sized chunks, and the resulting sequence of block tracks can then be merged into a track for the entire untrimmed DB with Catrack.

12. Catrack [-vfd] <path:db|dam> <track:name> ...

Find all block tracks of the form .<path>.#.<track>... and concatenate them into a single track, .<path>.<track>..., for the given DB or DAM. Do so for each track name present on the command line.  The block track files must all encode the same kind of track data (this is checked), and the files must exist for block 1, 2, 3, ... up to the last block number. If the -f option is set, then the concatenation takes place regardless of whether or not the single, combined track already exists or not. If the -d option is set then every block track is removed after the successful construction of the combined track.

13. DBshow [-unqaUQA] [-w<int(80)>] [-m<mask>]+
                      <path:db|dam> [ <reads:FILE> | <reads:range> ... ]

Displays the requested reads in the database <path>.db or <path>.dam. By default the command applies to the trimmed database, but if -u is set then the entire DB is used. If no read arguments are given then every read in the database or database block is displayed. Otherwise the input file or the list of supplied integer ranges give the ordinal positions in the actively loaded portion of the db. In the case of a file, it should simply contain a read index, one per line. In the other case, a read range is either a lone integer or the symbol $, in which case the read range consists of just that read (the last read in the database if $). One may also give two positive integers separated by a dash to indicate a range of integers, where again a $ represents the index of the last read in the actively loaded db. For example, 1 3-5 $ displays reads 1, 3, 4, 5, and the last read in the active db. As another example, 1-$ displays every read in the active db (the default).

By default a .fasta file of the read sequences is displayed. If the -q option is set and the DB is a Q-DB, then the QV streams are also displayed in a non-standard modification of the fasta format. Similarly, if the -a option is set and the DB is an A-DB, then the pulse width stream is also displayed in a non-standard format. If the -n option is set then the DNA sequence is not displayed. If the -Q option is set then a .quiva file of the selected reads is displayed and all other options except -u and -U are ignored. If the -A option is set then a .arrow file of the selected reads is displayed and all other options except -u and -w are ignored.

If one or more masks are set with the -m option then the track intervals are also displayed in an additional header line and the bases within an interval are displayed in the case opposite that used for all the other bases. By default the output sequences are in lower case and 80 chars per line. The -U option specifies upper case should be used, and the characters per line, or line width, can be set to any positive value with the -w option.

The .fasta, .quiva, and .arrow files that are output can be used to build a new DB with fasta2DB, quiva2D, and arrow2DB, giving one a simple way to make a DB of a subset of the reads for testing purposes.

14. DBdump [-rhsaqif] [-uU] [-m<mask>]+
                      <path:db|dam> [ <reads:FILE> | <reads:range> ... ]

Like DBshow, DBdump allows one to display a subset of the reads in the DB and select which information to show about them including any mask tracks. The difference is that the information is written in a very simple "1-code" ASCII format that makes it easy for one to read and parse the information for further use. The option flags determine which items of information are output as follows:

• -r requests that each read number be displayed in an R-line (see below, useful if only a subset of reads is requested).

• -h requests the header information be output as the source file name on an H-line, the If the -d option is set then every block track is removed after the successful construction of the combined track.well # and pulse range on an L-line, and optionally the quality of the read if given on a Q-line.

• -s requests the sequence be output on an S-line.

• -a requests the Arrow information be output as a pulse-width string on an A-line and the 4 SNR channel values on an N-line,

• -q requests that the 5 Quiver quality streams be output on d-, c-, i-, m-, and s-lines.

• -i requests that the intrinsic quality values be output on an I-line.

• -f requests the source file name is output just before the first read data in the file on a F-line.

• -m<track> requests that mask <track> be output on a T-line.

Set -u if you want data from the untrimmed database (the default is trimmed) and set -U if you'd like upper-case letter used in the DNA sequence strings.

The format is very simple. A requested unit of information occurs on a line. The first character of every line is a "1-code" character that tells you what information to expect on the line. The rest of the line contains the information where each item is separated by a single blank space. Strings are output as first an integer giving the length of the string, a blank space, and then the string terminated by a new-line. Intrinsic quality values are between 0 and 50, inclusive, and a vector of said are displayed as an alphabetic string where 'a' is 0, 'b' is '1', ... 'z' is 25, 'A' is 26, 'B' is 27, ... and 'Y' is 50. The set of all possible lines is as follows:

    R #              - read number
    H # string       - original file name string (header)
    L # # #          - location: well, pulse start, pulse end
    Q #              - quality of read (#/1000)
    N # # # #        - SNR of ACGT channels (#/100)
    Tx #n (#b #e)^#n - x'th track on command line, #n intervals all on same line
    S # string       - sequence string
    A # string       - arrow pulse-width string
    I # string       - intrinsic quality vector (as an ASCII string)
    F # string       - name of source file of following data
    d # string       - Quiva deletion values (as an ASCII string)
    c # string       - Quiva deletion character string
    i # string       - Quiva insertion value string
    m # string       - Quiva merge value string
    s # string       - Quiva substitution value string
    + X #            - Total amount of X (X = H or S or I or F or R or M or T#)
    @ X #            - Maximum amount of X (X = H or S or I or F or T#)

1-code lines that begin with + or @ are always the first lines in the output. They give size information about what is contained in the output. That is '+ X #' gives the number of reads (X=R), the number of masks (X=M), or the total number of characters in all headers (X=H), sequences (X=S), intrinsic quality vectors (X=I), file names (X=F), or track (X=T#). And '@ X #' gives the maximum number of characters in any header (X=H), sequence (X=S), intrincic quality vector (X=I), names (X=F), or track (X=T#). The size numbers for the Quiva strings and Arrow pulse width strings are identical to that for the sequence as they are all of the same length for any given entry.

15a. DBa2b
15b. DBb2a

Pipes (stdin to stdout) that convert an ASCII output produced by DBdump into a compressed binary representation (DBa2b) and vice verse (DBb2a). The idea is to save disk space by keeping the dumps in a more compessed format.

16. DBstats [-nu] [-b<int(1000)] [-m<mask>]+ <path:db|dam>

Show overview statistics for all the reads in the trimmed data base <path>.db or <path>.dam, including a histogram of read lengths where the bucket size is set with the -b option (default 1000). If the -u option is given then the untrimmed database is summarized. If the -n option is given then the histogran of read lengths is not displayed. Any track such as a "dust" track that gives a series of intervals along the read can be specified with the -m option in which case a summary and a histogram of the interval lengths is displayed.

17. DBrm [-v] <path:db|dam> ...

Delete all the files for the given data bases. Do not use rm to remove a database, as there are at least two and often several secondary files for each DB including track files, and all of these are removed by DBrm. If the -v option is set then every file deleted is listed.

18. DBmv [-v] <old:db|dam> <new:db|dam>

Rename all the files for the data base old to use the new root. If the -v option is set then every file move is displayed.

19. DBwipe <path:db|dam>

Delete any Arrow or Quiver data from the given databases. This removes the .arw or .qvs file and resets information in the .idx file containing information for Arrow or Quiver. Basically, converts an A-DB or Q-DB back to a simple S-DB.

20.  simulator <genome:dam> [-CU] [-m<int(10000)>] [-s<int(2000)>] [-e<double(.15)]
                                  [-c<double(50.)>] [-f<double(.5)>] [-x<int(4000)>]
                                  [-w<int(80)>] [-r<int>] [-M<file>]

In addition to the DB commands we include here, somewhat tangentially, a simple simulator that generates synthetic reads over a given genome reference contained in a supplied .dam DB. The simulator first reconstitutes the scaffolds of the reference genome and fills in their gaps (a run of N's in .fasta format indicating the estimate gap length) with a random sequence that follows the base distribution of the contigs. It will then sample reads from these scaffold sequences.

The simulator generates sample reads of mean length -m from a log-normal length distribution with standard deviation -s, but ignores reads of length less than -x. It collects enough reads to cover the genome -c times and Introduces -e fraction errors into each read where the ratio of insertions, deletions, and substitutions are set by defined constants INS_RATE (default 73%) and DEL_RATE (default 20%) within generate.c. One can control the rate at which reads are picked from the forward and reverse strands with the -f option. The -r option seeds the random number generator for the generation process so that one can reproducibly generate the same dataset. If this parameter is missing, then the job id of the invocation seeds the random number generator effectively guaranteeing a different sampling with each invocation.

The output is sent to the standard output (i.e. it is a UNIX pipe). The output is in Pacbio .fasta format suitable as input to fasta2DB. Uppercase letters are used if the -U option is given, and the width of each line can be controlled with the -w option.

Finally, the -M option requests that the scaffold and coordinates within said scaffold from which each read has been sampled are written to the indicated file, one line per read, ASCII encoded. This "map" file essential tells one where every read belongs in an assembly and is very useful for debugging and testing purposes. If the map line for a read is say 's b e' then if b < e the read is a perturbed copy of s[b,e] in the forward direction, and a perturbed copy s[e,b] in the reverse direction otherwise.

21. rangen <genlen:double> [-U] [-b<double(.5)>] [-w<int(80)>] [-r<int>]

Generate a random DNA sequence of length genlen*1Mbp that has an AT-bias of -b. Output the sequence to the standard output in .fasta format. Use uppercase letters if -U is set and -w base pairs per line (default 80). The result can then be converted into a .dam DB and given to the simulator to create a read database over a random synthetic sequence. The -r option seeds the random number generator for the generation process so that one can reproducibly generate the same sequence. If this parameter is missing, then the job id of the invocation seeds the random number generator effectively guaranteeing a different sequence with each invocation.

Example: A small complete example of most of the commands above.

> rangen 1.0 >R.fasta           //  Generate a randome 1Mbp sequence R.fasta
> fasta2DAM R R.fasta           //  Load it into a .dam DB R.dam
> simulator R -c20. >G.fasta    //  Sample a 20x data sets of the random geneome R
> fasta2DB G G.fasta            //  Create a compressed data base of the reads, G.db
> rm G.fasta                    //  Redundant, recreate any time with "DB2fasta G"
> DBsplit -s11 G                //  Split G into 2 parts of size ~ 11MB each
> DBdust G.1                    //  Produce a "dust" track on each part
> DBdust G.2
> Catrack G dust                //  Create one track for all of the DB
> rm .G.*.dust.*                //  Clean up the sub-tracks
> DBstats -mdust G              //  Take a look at the statistics for the database

Statistics for all reads in the data set

          1,836 reads        out of           1,836  (100.0%)
     20,007,090 base pairs   out of      20,007,090  (100.0%)

         10,897 average read length
          2,192 standard deviation

  Base composition: 0.250(A) 0.250(C) 0.250(G) 0.250(T)

  Distribution of Read Lengths (Bin size = 1,000)

        Bin:      Count  % Reads  % Bases     Average
     22,000:          1      0.1      0.1       22654
     21,000:          0      0.1      0.1       22654
     20,000:          1      0.1      0.2       21355
     19,000:          0      0.1      0.2       21355
     18,000:          4      0.3      0.6       19489
     17,000:          8      0.8      1.3       18374
     16,000:         19      1.8      2.8       17231
     15,000:         43      4.1      6.2       16253
     14,000:         81      8.6     12.0       15341
     13,000:        146     16.5     21.9       14428
     12,000:        200     27.4     34.4       13664
     11,000:        315     44.6     52.4       12824
     10,000:        357     64.0     71.2       12126
      9,000:        306     80.7     85.8       11586
      8,000:        211     92.2     94.8       11208
      7,000:         95     97.3     98.4       11017
      6,000:         43     99.7     99.8       10914
      5,000:          6    100.0    100.0       10897


Statistics for dust-track

  There are 158 intervals totaling 1,820 bases (0.0% of all data)

  Distribution of dust intervals (Bin size = 1,000)

        Bin:      Count  % Intervals  % Bases     Average
          0:        158        100.0    100.0          11

> ls -al
total 66518744
drwxr-xr-x+ 177 myersg  staff        6018 Mar  2 13:28 .
drwxr-xr-x+  20 myersg  staff         680 Feb 26 19:52 ..
-rw-r--r--+   1 myersg  staff     5002464 Mar  2 13:28 .G.bps
-rw-r--r--+   1 myersg  staff       14704 Mar  2 13:28 .G.dust.anno
-rw-r--r--+   1 myersg  staff        1264 Mar  2 13:28 .G.dust.data
-rw-r--r--+   1 myersg  staff       73552 Mar  2 13:28 .G.idx
-rw-r--r--+   1 myersg  staff         162 Mar  2 13:28 G.db
> cat G.db
files =         1
       1836 G Sim
blocks =         2
size =        11 cutoff =         0 all = 0
         0         0
      1011      1011
      1836      1836