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Resource Name
DINDEL
RRID:SCR_001827 RRID Copied      
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DINDEL (RRID:SCR_001827)
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Resource Information

URL: http://www.sanger.ac.uk/science/tools/dindel

Proper Citation: DINDEL (RRID:SCR_001827)

Description: THIS RESOURCE IS NO LONGER IN SERVICE. Documented on March 7,2024. Software program for calling small indels from short-read sequence data ("next generation sequence data"). It is currently designed to handle only Illumina data. Dindel takes BAM files with mapped Illumina read data and enables researchers to detect small indels and produce a VCF file of all the variant calls. It has been written in C++ and can be used on Linux-based and Mac computers (it has not been tested on Windows operating systems).

Abbreviations: Dindel

Synonyms: Dindel: Accurate indel calls from short-read data

Resource Type: software resource, software application

Defining Citation: PMID:20980555, DOI:10.1101/gr.112326.110

Keywords: indel, short-read, next generation sequence, illumina, gene, genetic, genomic, c++, linux, macos, bio.tools

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This resource

is listed by

OMICtools

is listed by

Genetic Analysis Software

is listed by

bio.tools

is listed by

Debian

has parent organization

Wellcome Trust Sanger Institute; Hinxton; United Kingdom

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Data and Source Information