bmc genomics trang 14 tải miễn phí từ TAILIEUCHUNG

"bmc genomics" trang 14 - tải miễn phí từ Tailieuchung

A pan-cancer somatic mutation embedding using autoencoders

A pan-cancer somatic mutation embedding using autoencoders

10 37 1

Rare variant phasing using paired tumor: Normal sequence data

Rare variant phasing using paired tumor: Normal sequence data

11 61 1

Aneuvis: Web-based exploration of numerical chromosomal variation in single cells

Aneuvis: Web-based exploration of numerical chromosomal variation in single cells

10 28 1

Shared data science infrastructure for genomics data

Shared data science infrastructure for genomics data

13 43 1

Barcode identification for single cell genomics

Barcode identification for single cell genomics

9 71 1

SV-Pop: Population-based structural variant analysis and visualization

SV-Pop: Population-based structural variant analysis and visualization

4 49 1

Developing reproducible bioinformatics analysis workflows for heterogeneous computing environments to support African genomics

Developing reproducible bioinformatics analysis workflows for heterogeneous computing environments to support African genomics

13 46 1

Evaluating methods of inferring gene regulatory networks highlights their lack of performance for single cell gene expression data

Evaluating methods of inferring gene regulatory networks highlights their lack of performance for single cell gene expression data

21 34 1

Mutational Signatures in Cancer (MuSiCa): A web application to implement mutational signatures analysis in cancer samples

Mutational Signatures in Cancer (MuSiCa): A web application to implement mutational signatures analysis in cancer samples

6 47 1

Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios

Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios

12 30 1

Rscreenorm: Normalization of CRISPR and siRNA screen data for more reproducible hit selection

Rscreenorm: Normalization of CRISPR and siRNA screen data for more reproducible hit selection

12 47 1

Inferring synteny between genome assemblies: A systematic evaluation

Inferring synteny between genome assemblies: A systematic evaluation

13 51 1

GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases

GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases

6 49 1

Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Germline contamination and leakage in whole genome somatic single nucleotide variant detection

9 41 1

ClustAGE: A tool for clustering and distribution analysis of bacterial accessory genomic elements

ClustAGE: A tool for clustering and distribution analysis of bacterial accessory genomic elements

12 29 1

Integrative analysis and machine learning on cancer genomics data using the Cancer Systems Biology Database (CancerSysDB)

Integrative analysis and machine learning on cancer genomics data using the Cancer Systems Biology Database (CancerSysDB)

10 54 1

Suggested mechanisms for Zika virus causing microcephaly: What do the genomes tell us

Suggested mechanisms for Zika virus causing microcephaly: What do the genomes tell us

12 26 1

SparkBLAST: Scalable BLAST processing using in-memory operations

SparkBLAST: Scalable BLAST processing using in-memory operations

13 33 1

Investigating reproducibility and tracking provenance – A genomic workflow case study

Investigating reproducibility and tracking provenance – A genomic workflow case study

14 66 1

CRISPulator: A discrete simulation tool for pooled genetic screens

CRISPulator: A discrete simulation tool for pooled genetic screens

12 23 1

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