"Single sequencing" trang 1 - tải miễn phí từ tailieunhanh
SMOOTH-seq: Single-cell genome sequencing of human cells on a thirdgeneration sequencing platform

SMOOTH-seq: Single-cell genome sequencing of human cells on a thirdgeneration sequencing platform
19    52    1
Single-cell characterization of CRISPRmodified transcript isoforms with nanopore sequencing

Single-cell characterization of CRISPRmodified transcript isoforms with nanopore sequencing
16    64    1
Learning mutational graphs of individual tumour evolution from single-cell and multi-region sequencing data

Learning mutational graphs of individual tumour evolution from single-cell and multi-region sequencing data
13    55    1
Eleven grand challenges in single-cell data science

Eleven grand challenges in single-cell data science
35    64    1
Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing

Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing
9    30    1
Comparative analysis of sequencing technologies for single-cell transcriptomics

Comparative analysis of sequencing technologies for single-cell transcriptomics
8    26    1
Single Cell Explorer, collaboration-driven tools to leverage large-scale single cell RNA-seq data

Single Cell Explorer, collaboration-driven tools to leverage large-scale single cell RNA-seq data
8    37    1
Multi-region and single-cell sequencing reveal variable genomic heterogeneity in rectal cancer

Multi-region and single-cell sequencing reveal variable genomic heterogeneity in rectal cancer
11    81    1
SCSIM: Jointly simulating correlated single-cell and bulk next-generation DNA sequencing data

SCSIM: Jointly simulating correlated single-cell and bulk next-generation DNA sequencing data
10    72    1
SmsMap: Mapping single molecule sequencing reads by locating the alignment starting positions

SmsMap: Mapping single molecule sequencing reads by locating the alignment starting positions
15    50    1
DrImpute: Imputing dropout events in single cell RNA sequencing data

DrImpute: Imputing dropout events in single cell RNA sequencing data
10    74    1
Dual indexed library design enables compatibility of in-Drop single-cell RNAsequencing with exAMP chemistry sequencing platforms

Dual indexed library design enables compatibility of in-Drop single-cell RNAsequencing with exAMP chemistry sequencing platforms
15    24    2
Millefy: Visualizing cell-to-cell heterogeneity in read coverage of single-cell RNA sequencing datasets

Millefy: Visualizing cell-to-cell heterogeneity in read coverage of single-cell RNA sequencing datasets
10    47    2
Combining next-generation sequencing and single-molecule sequencing to explore brown plant hopper responses to contrasting genotypes of japonica rice

Combining next-generation sequencing and single-molecule sequencing to explore brown plant hopper responses to contrasting genotypes of japonica rice
18    32    1
A systematic evaluation of single-cell RNA-sequencing imputation methods

A systematic evaluation of single-cell RNA-sequencing imputation methods
30    49    1
CSS: Cluster similarity spectrum integration of single-cell genomics data

CSS: Cluster similarity spectrum integration of single-cell genomics data
21    47    1
Systematic comparative analysis of singlenucleotide variant detection methods from single-cell RNA sequencing data

Systematic comparative analysis of singlenucleotide variant detection methods from single-cell RNA sequencing data
15    67    3
VIPER: Variability-preserving imputation for accurate gene expression recovery in single-cell RNA sequencing studies

VIPER: Variability-preserving imputation for accurate gene expression recovery in single-cell RNA sequencing studies
15    23    1
Ebook Principles of sequencing and scheduling: Part 1

Ebook Principles of sequencing and scheduling: Part 1
215    11    1
DdClone: Joint statistical inference of clonal populations from single cell and bulk tumour sequencing data

DdClone: Joint statistical inference of clonal populations from single cell and bulk tumour sequencing data
18    53    3