Sequence variant trang 1 tải miễn phí từ TAILIEUCHUNG

"Sequence variant" trang 1 - tải miễn phí từ Tailieuchung

Variant effect predictions capture some aspects of deep mutational scanning experiments

Variant effect predictions capture some aspects of deep mutational scanning experiments

12 28 1

Evaluation of variant calling tools for large plant genome re-sequencing

Evaluation of variant calling tools for large plant genome re-sequencing

16 48 1

ISVASE: Identification of sequence variant associated with splicing event using RNAseq data

ISVASE: Identification of sequence variant associated with splicing event using RNAseq data

7 52 1

Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery

Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery

27 40 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 58 3

Rare variant phasing using paired tumor: Normal sequence data

Rare variant phasing using paired tumor: Normal sequence data

11 61 1

Predicting variant deleteriousness in non-human species: Applying the CADD approach in mouse

Predicting variant deleteriousness in non-human species: Applying the CADD approach in mouse

10 38 1

Recurrent miscalling of missense variation from short-read genome sequence data

Recurrent miscalling of missense variation from short-read genome sequence data

9 33 1

Báo cáo y học: "Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities"

12 29 0

What is new and relevant for sequencing-based microbiome research? A mini-review

What is new and relevant for sequencing-based microbiome research? A mini-review

8 50 0

MC-GenomeKey: A multicloud system for the detection and annotation of genomic variants

MC-GenomeKey: A multicloud system for the detection and annotation of genomic variants

14 62 1

An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

7 20 1

Evaluation of variant detection software for pooled next-generation sequence data

Evaluation of variant detection software for pooled next-generation sequence data

9 21 1

Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline

Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline

11 43 1

SyRI: Finding genomic rearrangements and local sequence differences from wholegenome assemblies

SyRI: Finding genomic rearrangements and local sequence differences from wholegenome assemblies

13 39 3

DeepPVP: Phenotype-based prioritization of causative variants using deep learning

DeepPVP: Phenotype-based prioritization of causative variants using deep learning

8 24 1

Resolving complex structural genomic rearrangements using a randomized approach

Resolving complex structural genomic rearrangements using a randomized approach

13 23 1

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