Mlgt

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Application data

Created by Dave T. Gerrard
Biological application domain(s) genotyping, Targeted resequencing, Resequencing
Principal bioinformatics method(s) DNA sequence analysis, Error correction, Filtering, Sample Barcoding, Pooled samples, Read Alignment, Sequence analysis
Technology 454, pacific biosciences, Illumina?, Ion Torrent?
Created at University of Manchester
Maintained? Yes
Input format(s) FASTA
Output format(s) Tab-delimited file, RData, PDF
Software features Sequence assignment, sequence alignment, allignment error correction, variant counting, genotype calling, allele-matching
Programming language(s) R
Software libraries BLAST, MUSCLE
Licence GPL >=2
Operating system(s) Windows, UNIX, Mac OS X

Summary: Processing and analysis of high throughput, long-read (e.g. Roche 454) sequences generated from multiple loci and multiple biological samples. Sequences are assigned to their locus and sample of origin, aligned and trimmed. Where possible, genotypes are called and variants mapped to known alleles.

"Error: no local variable "counter" was set." is not a number.

Description

R package on CRAN http://cran.r-project.org/web/packages/mlgt/index.html

User README guide within package and here:- http://personalpages.manchester.ac.uk/staff/David.Gerrard/mlgtREADME.pdf





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