Methods to detect CNVs in the human genome-Reference-Cited by-同舟云学术

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Methods to detect CNVs in the human genome

Published:2008 Issue:1-4 Volume:123 Page:313-321
ISSN:1424-8581
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Aten E.,White S.J.,Kalf M.E.,Vossen R.H.A.M.,Thygesen H.H.,Ruivenkamp C.A.,Kriek M.,Breuning M.H.B.,den Dunnen J.T.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics,Molecular Biology

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. SavvyCNV: Genome-wide CNV calling from off-target reads;PLOS Computational Biology;2022-03-16

2. SavvyCNV: genome-wide CNV calling from off-target reads;2019-05-03

3. A multiplex ligation‑dependent probe amplification‑based next‑generation sequencing approach for the detection of copy number variations in the human genome;Molecular Medicine Reports;2018-10-24

4. Copy number variation related disease genes;Quantitative Biology;2018-05-11

5. Nanopore sequencing of complex genomic rearrangements in yeast reveals mechanisms of repeat-mediated double-strand break repair;Genome Research;2017-11-07

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