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URL: http://sourceforge.net/apps/mediawiki/breakway/index.php
Proper Citation: Breakway (RRID:SCR_001180)
Description: A suite of software programs that take aligned genomic data and report structural variation breakpoints. Features include: * Takes in BAM formatted input, the current standard for genomic alignments. * Compatible with standard output from major alignment algorithms such as BFAST, BWA, MAQ, et cetera. * Capable of analyzing data from any major platform--Solexa, SOLiD, 454, et cetera. * Empirically identifies structural variation breakpoints. * Highly specific analysis generates very few false positives. * Includes a suite of downstream tools for annotating identified breakpoints and reducing false positives.
Abbreviations: Breakway
Synonyms: Breakway: Identify Structural Variations in Genomic Data
Resource Type: software resource
Defining Citation: PMID:20126413
Keywords: genome, structural variation, breakpoint
Availability: Free, Available for download, Freely available
Resource Name: Breakway
Resource ID: SCR_001180
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400