"sequencing information" trang 12 - tải miễn phí từ tailieuXANH
CIPR: A web-based R/shiny app and R package to annotate cell clusters in single cell RNA sequencing experiments

CIPR: A web-based R/shiny app and R package to annotate cell clusters in single cell RNA sequencing experiments
15    153    0
PVAmpliconFinder: A workflow for the identification of human papillomaviruses from high-throughput amplicon sequencing

PVAmpliconFinder: A workflow for the identification of human papillomaviruses from high-throughput amplicon sequencing
18    76    0
DUGMO: Tool for the detection of unknown genetically modified organisms with highthroughput sequencing data for pure bacterial samples

DUGMO: Tool for the detection of unknown genetically modified organisms with highthroughput sequencing data for pure bacterial samples
17    60    0
SOAPTyping: An open-source and crossplatform tool for sequence-based typing for HLA class I and II alleles

SOAPTyping: An open-source and crossplatform tool for sequence-based typing for HLA class I and II alleles
9    68    0
A sparse Bayesian factor model for the construction of gene co-expression networks from single-cell RNA sequencing count data

A sparse Bayesian factor model for the construction of gene co-expression networks from single-cell RNA sequencing count data
19    62    0
FQStat: A parallel architecture for very highspeed assessment of sequencing quality metrics

FQStat: A parallel architecture for very highspeed assessment of sequencing quality metrics
10    53    0
GenePy - a score for estimating gene pathogenicity in individuals using nextgeneration sequencing data

GenePy - a score for estimating gene pathogenicity in individuals using nextgeneration sequencing data
15    49    0
A comparison of three programming languages for a full-fledged next-generation sequencing tool

A comparison of three programming languages for a full-fledged next-generation sequencing tool
10    58    0
A multivariate Poisson-log normal mixture model for clustering transcriptome sequencing data

A multivariate Poisson-log normal mixture model for clustering transcriptome sequencing data
11    97    0
Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data

Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data
11    55    0
FastProNGS: Fast preprocessing of nextgeneration sequencing reads

FastProNGS: Fast preprocessing of nextgeneration sequencing reads
6    153    0
Polled Digital Cell Sorter (p-DCS): Automatic identification of hematological cell types from single cell RNA-sequencing clusters

Polled Digital Cell Sorter (p-DCS): Automatic identification of hematological cell types from single cell RNA-sequencing clusters
16    65    0
FastqCleaner: An interactive Bioconductor application for quality-control, filtering and trimming of FASTQ files

FastqCleaner: An interactive Bioconductor application for quality-control, filtering and trimming of FASTQ files
7    91    0
SLIM: A flexible web application for the reproducible processing of environmental DNA metabarcoding data

SLIM: A flexible web application for the reproducible processing of environmental DNA metabarcoding data
6    48    0
Comparing the performance of selected variant callers using synthetic data and genome segmentation

Comparing the performance of selected variant callers using synthetic data and genome segmentation
11    52    0
BiSpark: A Spark-based highly scalable aligner for bisulfite sequencing data

BiSpark: A Spark-based highly scalable aligner for bisulfite sequencing data
9    52    1
DiNAMO: Highly sensitive DNA motif discovery in high-throughput sequencing data

DiNAMO: Highly sensitive DNA motif discovery in high-throughput sequencing data
10    51    0
BrownieAligner: Accurate alignment of Illumina sequencing data to de Bruijn graphs

BrownieAligner: Accurate alignment of Illumina sequencing data to de Bruijn graphs
10    86    0
DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data
13    49    0
A fully automated pipeline for quantitative genotype calling from next generation sequencing data in autopolyploids

A fully automated pipeline for quantitative genotype calling from next generation sequencing data in autopolyploids
10    178    0
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