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Cited by in F6Publishing
For: Richmond PA, Av-Shalom TV, Fornes O, Modi B, Elliott AM, Wasserman WW. GeneBreaker: Variant simulation to improve the diagnosis of Mendelian rare genetic diseases. Hum Mutat 2021;42:346-58. [PMID: 33368787 DOI: 10.1002/humu.24163] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
Number Citing Articles
1 Richmond PA, Av-Shalom TV, Fornes O, Modi B, Elliott AM, Wasserman WW. GeneBreaker: Variant simulation to improve the diagnosis of Mendelian rare genetic diseases. Hum Mutat 2021;42:346-58. [PMID: 33368787 DOI: 10.1002/humu.24163] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
2 Maroilley T, Li X, Oldach M, Jean F, Stasiuk SJ, Tarailo-Graovac M. Deciphering complex genome rearrangements in C. elegans using short-read whole genome sequencing. Sci Rep 2021;11:18258. [PMID: 34521941 DOI: 10.1038/s41598-021-97764-9] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Sun TH, Shao YJ, Mao CL, Hung MN, Lo YY, Ko TM, Hsiao TH. A Novel Quality-Control Procedure to Improve the Accuracy of Rare Variant Calling in SNP Arrays. Front Genet 2021;12:736390. [PMID: 34764980 DOI: 10.3389/fgene.2021.736390] [Reference Citation Analysis]