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[ Source: smalt  ]

Package: smalt (0.7.6-13)

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Sequence Mapping and Alignment Tool

SMALT efficiently aligns DNA sequencing reads with a reference genome. Reads from a wide range of sequencing platforms, for example Illumina, Roche-454, Ion Torrent, PacBio or ABI-Sanger, can be processed including paired reads.

The software employs a perfect hash index of short words (< 20 nucleotides long), sampled at equidistant steps along the genomic reference sequences.

For each read, potentially matching segments in the reference are identified from seed matches in the index and subsequently aligned with the read using a banded Smith-Waterman algorithm.

The best gapped alignments of each read is reported including a score for the reliability of the best mapping. The user can adjust the trade-off between sensitivity and speed by tuning the length and spacing of the hashed words.

A mode for the detection of split (chimeric) reads is provided. Multi-threaded program execution is supported.

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Download smalt

Download for all available architectures
Architecture Package Size Installed Size Files
alpha (unofficial port) 107.4 kB342.0 kB [list of files]
amd64 112.1 kB306.0 kB [list of files]
arm64 102.1 kB342.0 kB [list of files]
armel 97.2 kB272.0 kB [list of files]
armhf 95.9 kB200.0 kB [list of files]
hppa (unofficial port) 110.0 kB298.0 kB [list of files]
i386 124.1 kB344.0 kB [list of files]
ia64 (unofficial port) 143.4 kB547.0 kB [list of files]
m68k (unofficial port) 96.0 kB268.0 kB [list of files]
mips64el 106.4 kB362.0 kB [list of files]
ppc64 (unofficial port) 122.6 kB534.0 kB [list of files]
ppc64el 123.2 kB406.0 kB [list of files]
riscv64 112.6 kB250.0 kB [list of files]
s390x 113.7 kB326.0 kB [list of files]
sh4 (unofficial port) 119.7 kB276.0 kB [list of files]
sparc64 (unofficial port) 91.4 kB2,073.0 kB [list of files]
x32 (unofficial port) 111.7 kB296.0 kB [list of files]