Best practices for variant calling in clinical seq：Best practices for variant calling in clinical sequencing.
Best practices for variant calling in clinical sequencing.
由DCKoboldt著作·2020·被引用312次—Title:Bestpracticesforvariantcallinginclinicalsequencing.;Language:English;Authors:Koboldt,DanielC.·(AUTHOR)Daniel.Koboldt@nationwidechildrens.。其他文章還包含有：「Bestpracticesforvariantcallinginclinicalsequencing」、「Bestpracticesforvariantcallinginclinicalsequencing」、「Bestpracticesfortheinterpretationandreportingofclinical...」、「(PDF)Bestpracticesforv...
查看更多 離開網站
Best practices for variant calling in clinical sequencing
https://genomemedicine.biomedc
Variant alleles should be supported by reads on both strands with no apparent bias in read position, base quality, or mapping quality. High- ...
Best practices for variant calling in clinical sequencing
https://www.ncbi.nlm.nih.gov
Variant alleles should be supported by reads on both strands with no apparent bias in read position, base quality, or mapping quality. High- ...
Best practices for the interpretation and reporting of clinical ...
https://www.nature.com
Secondary analysis involves bioinformatic processes such as alignment of the raw sequence data to a genome reference, variant calling, and ...
(PDF) Best practices for variant calling in clinical sequencing
https://www.researchgate.net
The quality of NGS calls varies widely and is influenced by features like reference sequence characteristics, read depth, and mapping accuracy.