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A compilation and categorization of next-generation sequencing resources

DIAL - De novo Identification of Alleles

Tool nameDIAL - De novo Identification of Alleles
URL http://www.bx.psu.edu/miller_lab/
Important features1. DIAL (De novo Identification of Alleles), for identifying single-base substitutions between two closely related genomes without the help of a reference genome. 2. The method works even when the depth of coverage is insufficient for de novo assembly, and it can be extended to determine small insertions/deletions. 3. The use of DIAL to identify nucleotide differences among transcriptome sequences.
CitationsRatan A, Zhang Y, Hayes VM, Schuster SC, Miller W. Calling SNPs without a reference sequence. BMC Bioinformatics. 2010 Mar 15;11:130. PMID: 20230626
Year of publication2010
Rank by usage frequency100
CommentsRequires installation of LASTZ in the path.
FunctionSNP discovery
CategoryFree, Downloadable
LicenseMIT
Status
Input file formatSFF files for Roche 454, FASTQ for Illumina/Solexa
Output file format
Operating systemLinux 64 bit
Operating languageC, Python
PlatformIllumina/Solexa, Roche 454
Maintained byHeracle BioSoft
Downloadable file format
Submission file format

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