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=========================
= SMALT release history =
=========================
Release 0.7.6 (21 March 2014)
=============================
New features:
- For compilation on Intel's Many Integrated Cores
Architecture compile with ./configure --enable-mic
- Re-organised distributed tests.
- Minor changes allowing to switch between 0-based and 1-based offsets
for debugging (tracking) and to make vectorised alignment code
safer.
- Ammended installation instructions with the bambamc library.
Bug fixes:
- Fixed bug due to uninitialised re-used memory. This could result in
a flipped read orientation of a read (estimated incident rate
approx. 1 mate in 10^6 Illumina read pairs).
- fixed bug in 'smalt map -p' resulting in the "assertion failed"
error message. This could occur when a read aligned across two
successive sequences in the reference file for which the index was
constructed, and none of the matching segments exceeded the
threshold of the Smith-Waterman alignment score (set with -m).
- Fixed overcommitted memory in multi-threaded mode. The effect was
felt when using a large number of threads (> 16)., e.g. on intel MIC
cards.
- Fixed broken multi-threaded exection on Mac OSX (discovered on OSX
10.8.5) where the program could fail with 'assertion error' or
silently produce incomplete output.
=(smalt 0.7.6 21/03/2014 hp3)=
Release 0.7.5 (16 July 2013)
============================
New features:
- Changed buffering in multi-threaded mode to make code run more
efficient with a high number (>8) of threads. As a consequence,
the memory footprint increased compared to earlier versions.
Bug fixes:
- Fixed 'assertion failed' error that occurred with -p flag
and read pairs if no alignment was found for the mate with
the higher number of k-mer word hits in the hash index.
=(smalt 0.7.5 15/07/2013 hp3)=
Version 0.7.4.5 (09 July 2013)
==============================
- Fixed error message 'rmap.c:2048 ERROR: unknown error code' which
could occur with wide insert range boundaries (e.g. -i 80000).
Version 0.7.4.4 (25 June 2013)
==============================
- Fixed broken multi-threaded execution (option -n) on MacOSX (broken
since version 0.6.2). Program execution stopped prematurely and no
mappings were output. This was caused by the use of unnamed POSIX
semaphores (<semaphore.h>) that are not implemented on MacOSX.
- Modified configure script to generate 64-bit binaries on MacOSX Darwin
on x86_64 architecture.
Version 0.7.4.3 (20 June 2013)
==============================
- Fixed a bug that lead to the program terminating with a "assertion
failed" error message when one of the mates of a read pair had a
length shorter than the hashed words, but the other could be
aligned.
Version 0.7.4.2 (05 June 2013)
==============================
- Removed redundant code, added test data, moved code and repository
to SoureForge.
Version 0.7.4.1 (22 April 2013)
===============================
- Fixed a bug that led to alignments being missed in output generated
with the '-d' option. An alignment could be missed if it overlapped
with another, longer alignment even if that had a lower
Smith-Waterman score.
Release 0.7.4 (10 April 2013)
=============================
New features:
- added command line option '-S' for the specification of
alignment penalty scores.
Bug fixes:
- Fixed SAM input for orphan mates of read pairs.
- Fixed Multiple SAM/BAM lines with the 'secondary alignment' flag
unset. This occurred when using the '-d' option.
- Fixed spurious bug in CIGAR strings that denote mismatches by the
letter 'X' (e.g. with '-f smalt:x'). The read length represented by
the CIGAR string could be 1 bp less then the actual read length if
reads were mapped against > 512 reference sequences and could be
aligned across two successive reference sequences in the indexed
FASTA file. The faulty CIGAR string was issued when the read
alignment had a mismatch with the last base of the reference
sequence.
=(smalt 0.7.4 10/04/2013 hp3)=
Release 0.7.3 (15 March 2013)
=============================
New features:
- Added output of CIGAR strings with 'X' for mismatch in SAM and BAM
output formats with options '-f sam:x', '-f bam:x'
- Added 'NM' tag containing edit distance in SAM/BAM output formats to
comply with recommendations in SAM spec 1.4. Added @PG line to BAM
output.
- Updated interface to bambamc library version 0.0.42
Bug fixes:
- Fixed broken BAM output format when reads without base qualities
(FASTA format) were mapped.
- Fixed bug that scrambled BAM output format.
(output file was opened twice).
- Fixed bug in BAM ouptut format for paired reads: Bit 0x20 ("SEQ of
the next segment in the template being reversed") of the FLAG field
was set according to the 1st rather than the 2nd read of the pair.
- Fixed a bug when paired reads were mapped but only one of the reads
could be aligned with a Smith-Waterman score above the
threshold. The bug hat the program stopping with the error message
"assertion failed".
- Fixed segfault with explicit alignment output (option -a) and long
PacBio reads.
=(smalt 0.7.3 15/03/2013 hp3)=
Release 0.7.2 (22 February 2013)
================================
New features:
- Added @PG tag to SAM header.
- Overhauled online help options. smalt <task> without further option
prints short summary of available options.
- Added tests for BAM output format.
Bug fixes:
- Fixed BAM output format which was broken since 0.7.0.
Reference positions were off by +1 bp. CIGAR strings
were incorrect. Output was silent when smalt was compiled
without the bambamc library.
- Fixed missing SAM header for option -f 'sam' (default).
- Fixed sample task bailing out with an error message when there are
too few confident mappings and the histogram is therefore empty. Now
the program finishes without error messages but he output contains
line 'Histogram of insert sizes is empty'.
=(smalt 0.7.2 22/02/2013 hp3)=
Release 0.7.1 (29 January 2013)
===============================
New features:
- Adopted SAM spec 1.4 for the definition of insert sizes.
- Removed the restriction that the number of reference sequences
has to be representable by a signed 32-bit integer. The file format
for the compressed set of reference sequences changed.
- added support for reading gzipped FASTA/FASTQ files.
Bug fixes:
- Fixed inconsistent alignment (CIGAR) strings between mappings on the
forward strand the reference and alignments on the reverse
complement strand. The CIGAR string was inconsistent e.g. for
indels in homo-polymer runs, where the precises alingment was
ambiguous.
This caused problems when calling indels naively directly from the
mapping output without further processing, e.g. involving multiple
sequence alignment of the mapped reads in such regions.
- fixed broken '-p' flag for split read mapping.
- Fixed broken 'class' label in cigar output format. If
one of the mates was not mapped, the mapped mate was
assigned the label 'D' instead of the correct 'S'.
=(smalt 0.7.1 29/01/2013 hp3)=
Release 0.7.0.1 (05 November 2012)
==================================
- Fixed a number of bugs in verision 0.7.0 affecting indexing of and
mapping against contigs of an assembly. The index task crashed for
contigs and hits on the reverse complement strand were not correctly
collated.
- Fixed crashing check task.
- Progress reports are sent to stderr rather than previously stdout.
=(smalt 0.7.0.1 05/11/2012 hp3)=
Release 0.7.0 (18 October 2012 - withdrawn on 26/10/12)
=======================================================
- added support for reading SAM/BAM files (using German
Tischler's bambam libary and samtools). Added -F option to
specify input formats.
- Changed default behaviour: Where reads or read pairs have multiple
equivalent mappings a location is picked at random (as with the
option '-r 0'). The default output format is now SAM using soft
clipping. Output written to a file (option -o) in SAM format
contains the header.
- The option '-r -1' switches off random picking. Reads (pairs) with
multiple equivalent mappings are reported as 'not mapped'.
- When mapping paired reads, option '-d 0' now reports all possible
top ranking pairings.
- Alignments can now be output in BAM format (option '-f bam'). The
format specification for sam output can be extended by optional
keywords, e.g. '-f sam:nohead,clip' will omit the header and output
hard clipped read sequences.
=(smalt 0.7.0 18/10/2012 hp3)=
Release 0.6.4 (25 September 2012)
=================================
- fixed a bug in SAM output format for paired reads. The 'inferred
insert size' (field 9, ISIZE) was always set to 0 in version 0.6.3.
- fixed broken -a option. Progam bailed out with error message
"assertion failed" when an unmapped read was encountered.
=(smalt 0.6.4 25/09/2012 hp3)=
Release 0.6.3 (1 August 2012)
=============================
- Added '-O' flag which preserves the order of the reads in the input
files for the output when using multiple threads ('-n' option).
- Added GFF2 (Generic Feature Format, version 2) output format with the
option '-f gff'.
- Mapping with the option '-d 0' now outputs all possible mappings of
single reads with the best Smith-Waterman score. This option
overrides the '-r' option which triggers output of a single mapping
picked at random.
- Reduced memory footprint for multi-theaded mapping (option -n).
- Reduced the memory footprint when mapping paired reads with
very long insert sizes (> 100k pb).
- Fixed '-q' option which was not recognised for the 'map' task
resulting in the error message 'unknown option -q'.
- Fixed a bug in the explicit alignment output (-a option). The
alignment was scrambled for reads which aligned as the reverse
complement to the reference.
- Fixed a bug in the ouptput of multiple mappings with identical
Smith-Waterman scores. Multiple mappings were output even when one of
those mappings with identical Smith-Waterman scores had a higher
mapping quality than the rest. This happened when single reads were
mapped without the '-d' option specified
=(smalt 0.6.3 01/08/2012 hp3)=
Release 0.6.2 (21 May 2012)
===========================
- Fixed long-standing efficiency issues with multi-threaded execution
(-n option). The maximum number of additional threads that can be
forked is now 64 (used to be limited to 8).
WARNING: The order of the reads in the input files is no longer
preserved for the output. Mappings for read pairs are still output
in sucessive lines, though.
- Fixed broken 'sample' task. Program would stop with the message
'command line format error'.
- Fixed a bug affecting mapping to scaffolds. The bug could result in
missing partial alignments or stop of program execution with the
error message "ERROR: assertion failed".
=(smalt 0.6.2 21/05/2012 hp3)=
Release 0.6.1 (3 April 2012)
============================
- Corrected reading of hash-index files which was broken in version
0.6.0. The 'map' task halted with the error message 'error in file
format' for index files created with certain combinations of k-mer
lengths and sampling steps by the 'index' task. The error depended
also on the total length of reference sequences.
- Corrected 'check' task completing with 'end of file' error on
flawless input files.
=(smalt 0.6.1 03/04/2012 hp3)=
Release 0.6.0 (20 March 2012)
=============================
- Added 'check' and 'sample' tasks. Added '-g' option to the map task
for using insertion distribution generated with the 'sample' task.
- Ouput in SAM format now includes header lines.
- Fixed '-p' flag for partial mapping of reads which was broken for
single reads.
- Fixed 'assertion failed' error when attempting to map a read pair
where the sequences of both mates are shorter than the length k of
the k-mer words of the index.
=(smalt 0.6.0 20/03/2012 hp3)=
Release 0.5.8 (11 November 2011)
================================
- Added the option '-l pp' for paired read libraries where both
mates are sequenced on the same strand (e.g. 454 libraries)>
- Fixed segmentation fault error that could occur when multi-threading
('-n' option).
- Fixed a segmentation fault error when the hash index file could not
be found.
- Fixed program stopping prematurely with the error message 'Overflow
of Smith-Waterman score' that could occur when aligning very long
sequences (> 65536 bp).
=(smalt 0.5.8 11/11/2011 hp3)=
Release 0.5.7 (13 Sept 2011)
============================
- Introduced the 'R' label in SSAHA2 and CIGAR output formats obtained
without the '-r' option for reads that cannot be placed
unambiguously and until now were labelled 'N'. The label 'N' is now
restricted to reads for which no mapping location can be found.
- Fixed a bug in the output of paired reads where one mate maps to
multiple locations and the other mate can be mapped
unambigously. When mapping without the '-r' option, the unambiguous
mate was reported as 'unmapped'.
- Corrected mapping scores for paired reads which have were too
conservative (from version 0.5.4 onwards).
- Fixed a problem that occurred when there were more than 512
reference sequences in the index. The program could terminate with
the error message 'failure' if it encountered reads that had a long
sequence of nucleotides of unknown type (Ns) and their ends had
(spurious) alignments with reference sequences.
=(smalt 0.5.7 13/09/2011 hp3)=
Release 0.5.6 (2 Sept 2011)
===========================
- Added '-l' option specifying the type of read pair library used.
By default it is assumed that reads were produced by the illumina
paired-end (short insert) library protocol.
- Fixed a bug that caused an unnessecary large number of alignments to
be carried out for long reads (>~1000 bp). This resulted in 3x speed up
for long PacBio reads. The sensitivity was also improved.
=(smalt 0.5.6 02/09/2011 hp3)=
Release 0.5.5 (5 July 2011)
===========================
- Fixed core dump that cold occur with read pairs when only a single
pair was detected wher one mate had a mapping quality score of 0.
=(smalt 0.5.5 05/07/2011 hp3)=
Release 0.5.4 (1 July 2011)
===========================
- Fixed bug in SAM output for mate pairs present in version 0.5.3
where the insert size was set to 0.
- The '-c' option an now no longer be used unless the '-x' flag is
also set. It interferes with the heuristics used to filter
potentially matching segments.
- Fixed a bug introduced with verision 0.5.2 where, on rare occasions
program execution would stop with the error message 'sequence too
short to be hashed'.
- Better calibration of mapping quality scores for paired reads.
=(smalt 0.5.4 01/07/2011 hp3)=
Release 0.5.3 (8 June 2011)
===========================
- New calibration of mapping scores of paired reads. Mapping scores
take into account the orientation of the mapped mates. SMALT expects
paired reads as input as they result from the Illumina paired-end
(PE) library for short insert lengths (gaps). Reads from Illumina
mate-pair (MP) libraries with long insert lengths would have to be
converted to PE format to ensure correct scoring. The same holds for
paired reads from other sequencing platforms.
- Improved sensitivity and accuracy of paired reads at somewhat (~20%)
decreased speed.
- Output of multi-threaded execution (option '-n') now preserves the
order of the reads in the input file.
- Fixed a problem with 'mapping category' labels for paired reads in
CIGAR format. One of the mates of a pair mapped not in the expected
orientation could be wrongly labelled as the mate of a 'proper' pair
('A' rather than 'C').
- Fixed 'Smith-Waterman score overflow' error that occurred with
sequences > 255 bp on MacOSX.
=(smalt 0.5.3 08/06/2011 hp3)=
Release 0.5.2 (28 March 2011)
=============================
- Fixed '-r' option for the random picking of on of a set of
multiple best mappings (broken in version 0.5.1).
- Increased accuracy for paired-end reads.
=(smalt 0.5.2 28/03/2011 hp3)=
Release 0.5.1 (04 March 2011)
=============================
- introduced '-y' option for a threshold in the minimum number of
identical nucleotides.
- Extended SSAHA2 output format (option -f ssaha2) by one field
specifying the length of the reference sequence to which the read is
aligned.
- Changed the parameters for the default paired-read mapping
strategy. As before, the read with the fewer k-mer hits is aligned
first. If the mapping quality score is above a certain threshold
(10), the mate is aligned in a restricted zone around the
first. Otherwise the mate is aligned indepentently. In this version,
the insert size distribution is not taken into account for the
mapping quality or paired reads.
- repaired broken '-p' flag. In the sam output format, the second
partial alignment now has the 'secondary alignment' bit-flag (0x100)
of the FLAG field set. In cigar and ssaha output formats such an
alignment is labelled with 'P'.
- Fixed a few issues with the -m option which was broken, e.g. for '-d
0' (default).
- -f 'samsoft' was broken for unmapped reads when input files where in
FASTA rather than in FASTQ format. In this case the field with the
quality strings was missing in the SAM line.
- Fixed error message ('assertion failed') with FASTA query sequences
(query sequence without base qualities)
- Fixed error message ('assertion failed') with certain combinations
of -k and -s parameters when indexing.
=(smalt 0.5.1 04/03/2011 hp3)=
Release 0.5.0 (25 January 2011)
===============================
New features:
- New -r option picks at random one of a set of multiple best
mappings. This is only active in paired-end mode or if '-d 0' is
used (the default).
- New -q option sets a threshold of the base qualities. K-mer words
with nucleotides that have a base quality below this threshold are
not looked up in the hash index.
- The -m option now specifies a 'hard' absolute threshold of the
Smith- Waterman (SW) score. If the score of the best alignment of a
reads falls below the threshold, the read is reported as 'not
mapped'. Previous versions always reported alignments with the
overall best SW score even if that score was below the threshold set
with -m ('soft' threshold).
Bug fixes:
- Fixed 'integer overflow' error that could occur when the total length
of concatenated reference sequences exceeded 2^32 bp and the number of
reference sequences exceeded 512.
- Fixed a memory leak with long query sequences (> 1024 nucleotides).
- Fixed a problem with the alignment of very short reads: Program
execution stopped with the error message "Assertion failed" if the
read length was less than k + 2*s, where s is the sampling step and
k the length (indexing parameters '-k' and '-s') of the hashed kmer
words.
=(smalt 0.5.0 25/01/2011 hp3)=
Release 0.4.3 (17 December 2010)
================================
- Fixed a problem with unreliable spurious alignments in version 0.4.2.
Now the minimum length of aligned read segments is given by the sum
of the legth of the hashed kmer words and the sampling step size
(indexing parameters '-k' and '-s').
- Fixed a bug with paired reads and an index generated with -s 1 that
could result in the program stopping with the error "assertion
failed". This was caused by an integer overflow during the
calculation of candidate locations for the 2nd aligned mate.
- Fixed 1-nucleotide glitches in the length of the aligned segments of
the query read (or the CIGAR string). This was a rare event
that could happen when mapping against a large number of contigs.
=(smalt 0.4.3 17/12/2010 hp3)=
Release 0.4.2 (9 December 2010)
===============================
- Reduced memory footprint for compression of sequences
while indexing.
- The format of the sequence file (extension *.sma) has changed.
Reading of the sequence file is backwards compatible with versions
0.3.x.
- SAM ouput now has the '/1' and '/2' suffices stripped from the read
names of paired reads (indicate the order of mates).
Read names are otherwise not checked by SMALT. This means the
program won't detect whether the two FASTQ input files (READ_FILE
and MATE_FILE), which contain the reads of 1st and 2nd mate, were
swapped. Neither will the program detect whether or not the two
input files are 'in-sync', i.e. whether the i-th read in READ_FILE
corresponds to (is the mate of) the i-th read in MATE_FILE. Two
files could be 'out-of-sync' e.g. because one of the files has an
additional single read erroneously inserted.
- Output lines printed to standard output are now preceded by a hash
('#') if they contain progress reports by the program. This is so
they easily can be parsed out when alignment coordinates are piped
to standard output rather than written to a file (with the option
'-o').
- Fixed core dump that occured when indexing reference sequences with a
total number of nucleotides exceeding 2^32.
- Fixed core dump occuring with ssaha output format ('-f ssaha' flag).
=(smalt 0.4.2 09/12/2010 hp3)=
Release 0.4.1 (10 November 2010)
===============================
- Accelerated mapping speeds particularly for long (> 500 nt) reads.
- Re-calibrated mapping quality scores for 100bp Illumina reads of the
human genome.
- Changed the default minimum score (19) to <wordlen> + nskip - 1.
- Fixed the '-w' option which was broken in versions 0.3.x
- Fixed a number of bugs due to unitialised memory. Premature stop of
execution with error messages or core dumps could occur in
multi-thread mode (-n) or with the option '-d -1' when aligning
sequences >~ 1000 nt in length.
=(smalt 0.4.1 10/11/2010 hp3)=
Release 0.4.0 (14 October 2010)
===============================
- Implemented support for k-mer words of up to 20 nucleotides and
reduced the memory and disk footprint of the hash index for smaller
genomes. The memory required for the construction of the hash index
was also reduced.
- The file format for the index (file name extension *.smi)
changed. Reading of hash indices is backward compatible with
versions 0.3.x.
- Increased speeds for Sanger capillary reads more than 5-fold over
versions 0.3.x.
- Fixed a bug in version 0.3.2 that occasionally resulted in the
program exiting with error messages when the number of reference
sequences exceeded 256. The bug was limited to query sequences
(reads) aligning across two reference sequences adjacent in the
FASTA file from which the hash index was built.
- Fixed a bug in version 0.3.2 which affected the way paired read
alignments with multiple best mappings were output with the -d 0
(default) option. Such read pairs should be reported as unmapped,
but the bug occasionally caused one of the mates being reported as
mapped to one of the possible locations with a mapping quality of 1.
=(smalt 0.4.0 14/10/2010 hp3)=
Release 0.3.2 (24 August 2010)
==============================
- Fixed broken alignment coordinates when reads aligned across two or
more successive sequences in the FASTA file of reference sequences.
This bug occurred when the hash index was constructed for more than
256 reference sequences.
- Fixed broken offsets of aligned segments of the query read which
occurred predominantly with capillary and 454 reads.
=(smalt 0.3.2 24/08/2010 hp3)=
Release 0.3.1 (23 July 2010)
============================
- Fixed an error message "assertion failed" that occurred with query
reads with degenerate hits (multiple best hits) if the base call
qualities where missing (input in FASTA rather than FASTQ format).
- Fixed an error message "could not open file" that occurred in
multi-threaded mode with the '-o <output file>' option.
- Fixed a racing condition in multi-threaded mode. The maximum number
of threads for the '-n' option was set to 8.
- Changed the way degenerate hits are output when single reads are
mapped with the -d 0 (default) option: reads with degenerate hits
are output as 'unmapped' unless -d <swdiff> with swdiff != 0 is
used. E.g. -d 1 will output all mapped locations with the same best
Smith-Waterman score.
=(smalt 0.3.1 23/07/2010 hp3)=
Release 0.3 (06 July 2010)
============================
- First public release of pre-compiled binaries
=(smalt 0.3 06/07/2010 hp3)=
|