whole genome sequencing trang 6 tải miễn phí từ TAILIEUCHUNG

"whole genome sequencing" trang 6 - tải miễn phí từ Tailieuchung

Flexible and efficient genome tiling design with penalized uniqueness score

Flexible and efficient genome tiling design with penalized uniqueness score

11 45 1

A first insight into the genome of Prototheca wickerhamii, a major causative agent of human protothecosis

A first insight into the genome of Prototheca wickerhamii, a major causative agent of human protothecosis

14 16 1

NanotatoR: A tool for enhanced annotation of genomic structural variants

NanotatoR: A tool for enhanced annotation of genomic structural variants

16 23 1

Multi-trait GWAS using imputed highdensity genotypes from whole-genome sequencing identifies genes associated with body traits in Nile tilapia

Multi-trait GWAS using imputed highdensity genotypes from whole-genome sequencing identifies genes associated with body traits in Nile tilapia

13 31 1

The core genome multi-locus sequence typing of Mycoplasma anserisalpingitidis

The core genome multi-locus sequence typing of Mycoplasma anserisalpingitidis

8 30 2

DAWN: A resource for yielding insights into the diversity among wheat genomes

DAWN: A resource for yielding insights into the diversity among wheat genomes

20 31 1

Complete genome sequence and identification of polyunsaturated fatty acid biosynthesis genes of the myxobacterium Minicystis rosea DSM 24000T

Complete genome sequence and identification of polyunsaturated fatty acid biosynthesis genes of the myxobacterium Minicystis rosea DSM 24000T

15 29 1

Complete genome sequencing of three human clinical isolates of Staphylococcus caprae reveals virulence factors similar to those of S. epidermidis and S. capitis

Complete genome sequencing of three human clinical isolates of Staphylococcus caprae reveals virulence factors similar to those of S. epidermidis and S. capitis

17 19 1

Low incidence of SNVs and indels in trio genomes of Cas9-mediated multiplex edited sheep

Low incidence of SNVs and indels in trio genomes of Cas9-mediated multiplex edited sheep

8 28 1

GT-WGS: An efficient and economic tool for large-scale WGS analyses based on the AWS cloud service

GT-WGS: An efficient and economic tool for large-scale WGS analyses based on the AWS cloud service

10 38 1

HiNT: A computational method for detecting copy number variations and translocations from Hi-C data

HiNT: A computational method for detecting copy number variations and translocations from Hi-C data

15 26 1

Identification of cell type-specific methylation signals in bulk whole genome bisulfite sequencing data

Identification of cell type-specific methylation signals in bulk whole genome bisulfite sequencing data

23 20 1

Dysregulation of cancer genes by recurrent intergenic fusions

Dysregulation of cancer genes by recurrent intergenic fusions

20 35 1

Straglr: Discovering and genotyping tandem repeat expansions using whole genome long-read sequences

Straglr: Discovering and genotyping tandem repeat expansions using whole genome long-read sequences

20 37 1

When (distant) relatives stay too long: Implications for cancer medicine

When (distant) relatives stay too long: Implications for cancer medicine

4 7 1

A comprehensive survey of the mutagenic impact of common cancer cytotoxics

A comprehensive survey of the mutagenic impact of common cancer cytotoxics

16 13 1

Sparse conserved under-methylated CpGs are associated with high-order chromatin structure

Sparse conserved under-methylated CpGs are associated with high-order chromatin structure

10 42 1

EpiG: Statistical inference and profiling of DNA methylation from whole-genome bisulfite sequencing data

EpiG: Statistical inference and profiling of DNA methylation from whole-genome bisulfite sequencing data

16 17 3

The evolution of CHROMOMETHYLASES and gene body DNA methylation in plants

The evolution of CHROMOMETHYLASES and gene body DNA methylation in plants

13 40 3

SEPATH: Benchmarking the search for pathogens in human tissue whole genome sequence data leads to template pipelines

SEPATH: Benchmarking the search for pathogens in human tissue whole genome sequence data leads to template pipelines

15 19 3

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