single sequencing trang 10 tải miễn phí từ TAILIEUCHUNG

"single sequencing" trang 10 - tải miễn phí từ Tailieuchung

Characterization of genetic aberrations in a single case of metastatic thymic adenocarcinoma

Characterization of genetic aberrations in a single case of metastatic thymic adenocarcinoma

12 59 1

Genome-wide association studies of seven agronomic traits under two sowing conditions in bread wheat

Genome-wide association studies of seven agronomic traits under two sowing conditions in bread wheat

18 33 1

First insight into the somatic mutation burden of neurofibromatosis type 2- associated grade I and grade II meningiomas: A case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation

First insight into the somatic mutation burden of neurofibromatosis type 2- associated grade I and grade II meningiomas: A case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation

10 64 1

Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma

Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma

9 73 1

Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing

Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing

12 22 1

Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads

Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads

9 66 1

RESCUE: Imputing dropout events in singlecell RNA-sequencing data

RESCUE: Imputing dropout events in singlecell RNA-sequencing data

11 24 1

Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites

Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites

13 33 1

Valection: Design optimization for validation and verification studies

Valection: Design optimization for validation and verification studies

11 62 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

DMRfinder: Efficiently identifying differentially methylated regions from MethylC-seq data

DMRfinder: Efficiently identifying differentially methylated regions from MethylC-seq data

8 65 1

Whole genome SNP genotype piecemeal imputation

Whole genome SNP genotype piecemeal imputation

11 35 1

PGen: Large-scale genomic variations analysis workflow and browser in SoyKB

PGen: Large-scale genomic variations analysis workflow and browser in SoyKB

10 37 1

Multi-CAR: A tool of contig scaffolding using multiple references

Multi-CAR: A tool of contig scaffolding using multiple references

8 48 1

Afull Bayesian partitionmodelfor identifying hypo- and hyper-methylated loci from single nucleotide resolution sequencing data

Afull Bayesian partitionmodelfor identifying hypo- and hyper-methylated loci from single nucleotide resolution sequencing data

13 34 1

DRUMS: Disk Repository with Update Management and Select option for high throughput sequencing data

DRUMS: Disk Repository with Update Management and Select option for high throughput sequencing data

9 51 1

Comparison of genotype clustering tools with rare variants

Comparison of genotype clustering tools with rare variants

12 60 1

Identification of pathogen genomic variants through an integrated pipeline

Identification of pathogen genomic variants through an integrated pipeline

14 22 1

Bayesian neural networks for detecting epistasis in genetic association studies

Bayesian neural networks for detecting epistasis in genetic association studies

12 29 1

SSPACE-LongRead: Scaffolding bacterial draft genomes using long read sequence information

SSPACE-LongRead: Scaffolding bacterial draft genomes using long read sequence information

9 22 1

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