Titlebook: Copy Number Variants; Methods and Protocol Derek M. Bickhart Book 2018 Springer Science+Business Media, LLC, part of Springer Nature 2018 P

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書目名稱Copy Number Variants影響因子(影響力)




書目名稱Copy Number Variants影響因子(影響力)學科排名




書目名稱Copy Number Variants網(wǎng)絡公開度




書目名稱Copy Number Variants網(wǎng)絡公開度學科排名




書目名稱Copy Number Variants被引頻次




書目名稱Copy Number Variants被引頻次學科排名




書目名稱Copy Number Variants年度引用




書目名稱Copy Number Variants年度引用學科排名




書目名稱Copy Number Variants讀者反饋




書目名稱Copy Number Variants讀者反饋學科排名

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1064-3745 tative and cutting-edge, .Copy Number Variants: Methods and Protocols .aims to provide guidance to Bioinformaticians and Molecular Biologists who are interested in identifying copy number variants (CNV) with a wide variety of experimental media978-1-4939-9359-8978-1-4939-8666-8Series ISSN 1064-3745 Series E-ISSN 1940-6029

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https://doi.org/10.1007/978-1-4302-0262-2a tool that incorporates read-pair and split-read signals to identify high confidence CNV regions in a sequenced sample. By combining two different structural variant (SV) signals in variant calling, RAPTR-SV enables the easy filtration of artifact CNV calls from large datasets.

連系

Use of RAPTR-SV to Identify SVs from Read Pairing and Split Read Signatures,a tool that incorporates read-pair and split-read signals to identify high confidence CNV regions in a sequenced sample. By combining two different structural variant (SV) signals in variant calling, RAPTR-SV enables the easy filtration of artifact CNV calls from large datasets.

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Book 2018y Number Variants: Methods and Protocols .aims to provide guidance to Bioinformaticians and Molecular Biologists who are interested in identifying copy number variants (CNV) with a wide variety of experimental media

SOB

https://doi.org/10.1007/978-1-4302-0262-2e fragment size and read length, which are limiting factors in read pair and split read analysis. Here we provide a guideline for a user friendly tool for detecting large segmental duplications and deletions that can also predict integer copy numbers for duplicated genes.

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