NGSanalyzer 1.0 – Identifying SNV and Indels from Short Read Sequence data

NGSanalyzer 1.0

:: DESCRIPTION

NGSanalyzer is a suit of tools for identifying SNV (single nucleotide variations) and indels (insertions and deletions) from short read sequence data.

::DEVELOPER

Laboratory for Medical Science Mathematics

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 NGSanalyzer

:: MORE INFORMATION

SNP2CAPS – SNP and INDEL Analysis Tool for CAPS Marker Development

SNP2CAPS

:: DESCRIPTION

SNP2CAPS facilitates the computational conversion of SNPs into CAPS markers. A simple algorithm involves the screening of multiply-aligned sequences for restriction sites followed by a selection pipeline that allows the deduction of CAPS candidates by the identification of putative alternative restriction sites.

::DEVELOPER

Thomas Thiel  at the IPK-Gatersleben

:: SCREENSHOTS

:: REQUIREMENTS

  • Windows / Linux/  MacOSX
  • Perl

:: DOWNLOAD

 SNP2CAPS

:: MORE INFORMATION

Citation

T. Thiel, R. Kota, I. Grosse, N. Stein, and A. Graner.
SNP2CAPS: a SNP and INDEL analysis tool for CAPS marker development.
Nucleic Acids Research, 32(1):e5, 2004.

MoDIL 1.1 – Detect INDEL Variation with Clone-end Sequencing

MoDIL 1.1

:: DESCRIPTION

MoDIL (Mixture of Distributions Indel Locator) is a novel method for finding medium sized indels from high throughput sequencing datasets.

::DEVELOPER

the Computational Biology Labat the University of Toronto’s Department of Computer Science.

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 MoDIL

:: MORE INFORMATION

Citation

Seunghak Lee, Fereydoun Hormozdiari, Can Alkan & Michael Brudno
MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions
Nature Methods 6, 473 – 474 (2009)