Downloading older version of a tool - Biostar: S Hello there, I am downloading this tool SMALT 0 5 8 but the current version is 0 7 6 Can you guide me how to download on conda using bioconda channel? I tried to find it on github and on conda but conda says the package isn't avaliable on the channels update:
BWA or SMALT mapping algorithm - Biostar: S So will other algorithms such bwa-mem or SMALT be better to use than bwa-aln? SMALT BWA • 4 2k views ADD COMMENT • link updated 3 3 years ago by Ram 45k • written 10 6 years ago by P NJ utrif; 50
Gpu-Blast Vs Smalt - Biostar: S Hi, I am wondering if anyone has compared Smalt vs Blast Two ways to use Smith-Waterman to map reads to a reference genome I recently got a hold of GPU-Blast and was wondering if it might go the same speed If so, would it have more optimal alignments?
SMALT aligner SAM clipping option? I am mapping my reads using smalt (for specific reasons) program and I am wondering if any one have come across smalt's sam output formatting options? you can specify format output with -f flag it also has some extensions i e -f sam:nohead:x:clip where x is for cigar string, nohead is for no headers and clip is for hard clipping
Getting Smalt to work with bambamc - Biostar: S Smalt requires bambamc to be able to work with BAM files Smalt is returning the error: smalt: error while loading shared libraries: libbambamc so 0: cannot open shared object file: No such file or directory
Long read alignment - biostars Smalt, BBmap and MUMmer are all claimed to work with PacBio reads, but I have not tried myself Finally, blast, lastz and blastz should also work provided that you use the right settings Probably I need to do a brief survey
Foss Equivalent To Clc Assembly Cell? - Biostar: S EDIT: for your application, you may try bwa-sw and smalt If the default configuration fails, you may consider to change the parameter to make them more sensitive (for bwa-sw, increase -z to -z10 or so)
multicuv error Could not find indexes I am trying to get new coordinated for my sequencing file so i tried to align my new version of the genomic file (TB927_v5 1) I used smalt to get sam file I converted my sam file into bam file using this command: samtools view -h -b -S out sam > out bam Next, i used to multicuv bedtools multicov -bams out bam -bed merged bed >nucleolus txt
Error using in Smalt aligner program It is a bug that is fixed in 0 7 6 version From the SMALT release history: 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
Split Read Mapping By Bwa And Bowtie2 - biostars Smalt might work for split alignment, but I am not sure, either EDIT: BTW, you may also try a new algorithm on the bwa mem branch that has a new component called mem In theory, it should be more sensitive than bwa-sw for your data, but that branch is only a week old and is unstable