Mercurial > repos > jpayne > seqsero_v2
diff README.md @ 0:4ff2aee11e5b
planemo upload
author | jpayne |
---|---|
date | Tue, 06 Nov 2018 09:45:57 -0500 |
parents | |
children |
line wrap: on
line diff
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/README.md Tue Nov 06 09:45:57 2018 -0500 @@ -0,0 +1,41 @@ +# SeqSero2 alpha-test version +Salmonella serotyping from genome sequencing data + + +# Introduction +SeqSero2 is a pipeline for Salmonella serotype determination from raw sequencing reads or genome assemblies. This is a alpha test version. For now, it can only accept separated paired-end reads. A web app will be available soon. + +# Dependencies +SeqSero depends on: + +1. Python 2.7 and [Biopython 1.65](http://biopython.org/wiki/Download); + +2. [Burrows-Wheeler Aligner](http://sourceforge.net/projects/bio-bwa/files/); + +3. [Samtools](http://sourceforge.net/projects/samtools/files/samtools/); + +4. [NCBI BLAST](https://blast.ncbi.nlm.nih.gov/Blast.cgi?PAGE_TYPE=BlastDocs&DOC_TYPE=Download); + +5. [SRA Toolkit](http://www.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?cmd=show&f=software&m=software&s=software); + +6. [SPAdes](http://bioinf.spbau.ru/spades); + +7. [Bedtools](http://bedtools.readthedocs.io/en/latest/). + +# Executing the code + Usage: SeqSero2.py + + -p <int> (number of threads, if p >4, only 4 threads will be used for assembly since the amount of extracted reads is small, default=1) + + -i <file> (/path/to/input/file; for now, SeqSero2 only accepts separated paired-end reads ) + + -b <string> (algorithms for bwa mapping; 'mem' for mem, 'sam' for samse/sampe; default=mem; optional; for now SeqSero2 is only optimized for "mem" mode) + +# Output +Upon executing the command, a directory named 'SeqSero_result_Time_your_run' will be created. Your result will be stored in 'Seqsero_result.txt' in that directory. And the assembled alleles can also be found in the directory. + +# Citation +Zhang S, Yin Y, Jones MB, Zhang Z, Deatherage Kaiser BL, Dinsmore BA, Fitzgerald C, Fields PI, Deng X. +Salmonella serotype determination utilizing high-throughput genome sequencing data. +**J Clin Microbiol.** 2015 May;53(5):1685-92.[PMID:25762776](http://jcm.asm.org/content/early/2015/03/05/JCM.00323-15) +