DOKK / manpages / debian 12 / lambda-align / lambda.1.en
LAMBDA(1) LAMBDA(1)

lambda - the Local Aligner for Massive Biological DatA

lambda [OPTIONS] -q QUERY.fasta -d DATABASE.fasta [-o output.m8]

Lambda is a local aligner optimized for many query sequences and searches in protein space. It is compatible to BLAST, but much faster than BLAST and many other comparable tools.

Detailed information is available in the wiki: <https://github.com/seqan/lambda/wiki>

Display the help message.
Display the help message with advanced options.
Turn this option off to disable version update notifications of the application. One of 1, ON, TRUE, T, YES, 0, OFF, FALSE, F, and NO. Default: 1.
Display version information.
Display long copyright information.
Display more/less diagnostic output during operation: 0 [only errors]; 1 [default]; 2 [+run-time, options and statistics]. In range [0..2]. Default: 1.

Query sequences. Valid filetypes are: .sam[.*], .raw[.*], .gbk[.*], .frn[.*], .fq[.*], .fna[.*], .ffn[.*], .fastq[.*], .fasta[.*], .faa[.*], .fa[.*], .embl[.*], and .bam, where * is any of the following extensions: gz, bz2, and bgzf for transparent (de)compression.
Path to original database sequences (a precomputed index with .sa or .fm needs to exist!). Valid filetypes are: .sam[.*], .raw[.*], .gbk[.*], .frn[.*], .fq[.*], .fna[.*], .ffn[.*], .fastq[.*], .fasta[.*], .faa[.*], .fa[.*], .embl[.*], and .bam, where * is any of the following extensions: gz, bz2, and bgzf for transparent (de)compression.
database index is in this format. One of sa and fm. Default: fm.

File to hold reports on hits (.m* are blastall -m* formats; .m8 is tab-seperated, .m9 is tab-seperated with with comments, .m0 is pairwise format). Valid filetypes are: .sam[.*], .m9[.*], .m8[.*], .m0[.*], and .bam, where * is any of the following extensions: gz, bz2, and bgzf for transparent (de)compression. Default: output.m8.
Print specified column combination and/or order (.m8 and .m9 outputs only); call -oc help for more details. Default: std.
Output only matches above this threshold (checked before e-value check). In range [0..100]. Default: 0.
Output only matches that score below this threshold. In range [0..inf]. Default: 0.1.
Print at most this number of matches per query. In range [1..inf]. Default: 500.
BAM files require all subject names to be written to the header. For SAM this is not required, so Lambda does not automatically do it to save space (especially for protein database this is a lot!). If you still want them with SAM, e.g. for better BAM compatibility, use this option. One of on and off. Default: off.
Write matching DNA subsequence into SAM/BAM file (BLASTN). For BLASTX and TBLASTX the matching protein sequence is "untranslated" and positions retransformed to the original sequence. For BLASTP and TBLASTN there is no DNA sequence so a "*" is written to the SEQ column. The matching protein sequence can be written as an optional tag, see --sam-bam-tags. If set to uniq than the sequence is omitted iff it is identical to the previous match's subsequence. One of always, uniq, and never. Default: uniq.
Write the specified optional columns to the SAM/BAM file. Call --sam-bam-tags help for more details. Default: AS NM ZE ZI ZF.
Whether to hard-clip or soft-clip the regions beyond the local match. Soft-clipping retains the full sequence in the output file, but obviously uses more space. One of hard and soft. Default: hard.

number of threads to run concurrently.
controls double-indexing. One of radix and none. Default: none.

Blast Operation Mode. One of blastn, blastp, blastx, tblastn, and tblastx. Default: blastx.
The translation table to use for nucl -> amino acid translation(not for BlastN, BlastP). See https://www.ncbi.nlm.nih.gov/Taxonomy/Utils/wprintgc.cgi?mode=c for ids (default is generic). Six frames are generated. Default: 1.
Alphabet Reduction for seeding phase (ignored for BLASTN). One of none and murphy10. Default: murphy10.

Length of the seeds (default = 14 for BLASTN). Default: 10.
Offset for seeding (if unset = seed-length, non-overlapping; default = 5 for BLASTN). Default: 10.
maximum seed distance. Default: 1.

evaluate score of a region NUM times the size of the seed before extension (0 -> no pre-scoring, 1 -> evaluate seed, n-> area around seed, as well; default = 1 if no reduction is used). In range [1..inf]. Default: 2.
minimum average score per position in pre-scoring region. Default: 2.
filter hits that will likely duplicate a match already found. One of on and off. Default: on.
If the maximum number of matches per query are found already, stop searching if the remaining realm looks unfeasable. One of on and off. Default: on.

use '45' for Blosum45; '62' for Blosum62 (default); '80' for Blosum80; [ignored for BlastN] Default: 62.
Score per gap character (default = -2 for BLASTN). Default: -1.
Additional cost for opening gap (default = -5 for BLASTN). Default: -11.
Match score [only BLASTN]) Default: 2.
Mismatch score [only BLASTN] Default: -3.

Stop Banded extension if score x below the maximum seen (-1 means no xdrop). In range [-1..inf]. Default: 30.
Size of the DP-band used in extension (-3 means log2 of query length; -2 means sqrt of query length; -1 means full dp; n means band of size 2n+1) In range [-3..inf]. Default: -3.

Tuning the seeding parameters and (de)activating alphabet reduction has a strong influence on both speed and sensitivity. We recommend the following alternative profiles for protein searches:

fast (high similarity): -ar none -sl 7 -sd 0

sensitive (lower similarity): -so 5

For further information see the wiki: <https://github.com/seqan/lambda/wiki>

lambda Copyright: 2013-2017 Hannes Hauswedell, released under the GNU GPL v3 (or later); 2016-2017 Knut Reinert and Freie Universität Berlin, released under the 3-clause-BSDL
SeqAn Copyright: 2006-2015 Knut Reinert, FU-Berlin; released under the 3-clause BSDL.
In your academic works please cite: Hauswedell et al (2014); doi: 10.1093/bioinformatics/btu439
For full copyright and/or warranty information see --copyright.

Feb 8 2020 lambda 1.0.2