"sequencing error" trang 14 - tải miễn phí từ tailieuXANH
SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data

SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data
9    57    0
LW-FQZip 2: A parallelized reference-based compression of FASTQ files

LW-FQZip 2: A parallelized reference-based compression of FASTQ files
8    66    0
MeFiT: Merging and filtering tool for illumina paired-end reads for 16S rRNA amplicon sequencing

MeFiT: Merging and filtering tool for illumina paired-end reads for 16S rRNA amplicon sequencing
6    62    0
Roar: Detecting alternative polyadenylation with standard mRNA sequencing libraries

Roar: Detecting alternative polyadenylation with standard mRNA sequencing libraries
9    48    0
Spectra library assisted de novo peptide sequencing for HCD and ETD spectra pairs

Spectra library assisted de novo peptide sequencing for HCD and ETD spectra pairs
7    49    0
Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers

Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers
15    69    0
NEAT: A framework for building fully automated NGS pipelines and analyses

NEAT: A framework for building fully automated NGS pipelines and analyses
9    86    0
ClinQC: A tool for quality control and cleaning of Sanger and NGS data in clinical research

ClinQC: A tool for quality control and cleaning of Sanger and NGS data in clinical research
9    123    0
ADEPT, a dynamic next generation sequencing data error-detection program with trimming

ADEPT, a dynamic next generation sequencing data error-detection program with trimming
7    80    0
Empirical estimation of sequencing error rates using smoothing splines

Empirical estimation of sequencing error rates using smoothing splines
11    81    0
A novel procedure on next generation sequencing data analysis using text mining algorithm

A novel procedure on next generation sequencing data analysis using text mining algorithm
15    100    0
Detection and sequence/structure mapping of biophysical constraints to protein variation in saturated mutational libraries and protein sequence alignments with a dedicated server

Detection and sequence/structure mapping of biophysical constraints to protein variation in saturated mutational libraries and protein sequence alignments with a dedicated server
13    63    0
Consistency of biological networks inferred from microarray and sequencing data

Consistency of biological networks inferred from microarray and sequencing data
10    169    0
An Atlas of annotations of Hydra vulgaris transcriptome

An Atlas of annotations of Hydra vulgaris transcriptome
7    62    0
CloneCNA: Detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

CloneCNA: Detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data
10    52    0
Analysis of amplicon-based NGS data from neurological disease gene panels: A new method for allele drop-out management

Analysis of amplicon-based NGS data from neurological disease gene panels: A new method for allele drop-out management
12    66    0
Optimized pipeline of MuTect and GATK tools to improve the detection of somatic single nucleotide polymorphisms in wholeexome sequencing data

Optimized pipeline of MuTect and GATK tools to improve the detection of somatic single nucleotide polymorphisms in wholeexome sequencing data
9    82    0
Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approaches

Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approaches
10    56    0
TRAPLINE: A standardized and automated pipeline for RNA sequencing data analysis, evaluation and annotation

TRAPLINE: A standardized and automated pipeline for RNA sequencing data analysis, evaluation and annotation
11    64    0
ContextMap 2: Fast and accurate context-based RNA-seq mapping

ContextMap 2: Fast and accurate context-based RNA-seq mapping
15    70    0
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