Variation calling trang 1 tải miễn phí từ tailieunhanh

"Variation calling" trang 1 - tải miễn phí từ tailieunhanh

Towards pan-genome read alignment to improve variation calling

Towards pan-genome read alignment to improve variation calling

8 60 1

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins

8 64 1

Removing reference bias and improving indel calling in ancient DNA data analysis by mapping to a sequence variation graph

Removing reference bias and improving indel calling in ancient DNA data analysis by mapping to a sequence variation graph

18 37 1

Conbase: A software for unsupervised discovery of clonal somatic mutations in single cells through read phasing

Conbase: A software for unsupervised discovery of clonal somatic mutations in single cells through read phasing

18 17 1

Evaluation of copy number variation detection for a SNP array platform

Evaluation of copy number variation detection for a SNP array platform

9 40 1

Gramtools enables multiscale variation analysis with genome graphs

Gramtools enables multiscale variation analysis with genome graphs

27 47 1

Paragraph: A graph-based structural variant genotyper for short-read sequence data

Paragraph: A graph-based structural variant genotyper for short-read sequence data

13 73 3

Deep sampling and pooled amplicon sequencing reveals hidden genic variation in heterogeneous rye accessions

Deep sampling and pooled amplicon sequencing reveals hidden genic variation in heterogeneous rye accessions

16 37 1

Streamlined computational pipeline for genetic background characterization of genetically engineered mice based on next generation sequencing data

Streamlined computational pipeline for genetic background characterization of genetically engineered mice based on next generation sequencing data

20 17 1