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Resource Name
inGAP
RRID:SCR_005261 RRID Copied      
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inGAP (RRID:SCR_005261)
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Resource Information

URL: http://ingap.sourceforge.net/

Proper Citation: inGAP (RRID:SCR_005261)

Description: Software mining pipeline guided by a Bayesian principle to detect single nucleotide polymorphisms, insertion and deletions by comparing high-throughput pyrosequencing reads with a reference genome of related organisms. This pipeline is extended to identify and visualize large-size structural variations, including insertions, deletions, inversions and translocations.

Abbreviations: inGAP

Synonyms: inGAP-sv, inGAP-sv: structural variation detection and visualization, integrative next-generation genome analysis pipeline

Resource Type: software resource

Keywords: structural variation, genome, next-generation sequence, genome analysis, alignment, single nucleotide polymorphism, insertion, deletion, indel, inversion, translocation, windows, linux, macos/x, bio.tools

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This resource

is listed by

OMICtools

is listed by

bio.tools

is listed by

Debian

has parent organization

SourceForge

has parent organization

Fudan University; Shanghai; China

has parent organization

Chinese Academy of Sciences; Beijing; China

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