"Paired end short reads" trang 1 - tải miễn phí từ tailieuXANH
Joining Illumina paired-end reads for classifying phylogenetic marker sequences

Joining Illumina paired-end reads for classifying phylogenetic marker sequences
13    62    0
NucBreak: Location of structural errors in a genome assembly by using paired-end Illumina reads

NucBreak: Location of structural errors in a genome assembly by using paired-end Illumina reads
11    50    0
Impact of quality trimming on the efficiency of reads joining and diversity analysis of Illumina paired-end reads in the context of QIIME1 and QIIME2 microbiome analysis frameworks

Impact of quality trimming on the efficiency of reads joining and diversity analysis of Illumina paired-end reads in the context of QIIME1 and QIIME2 microbiome analysis frameworks
10    101    0
NGmerge: Merging paired-end reads via novel empirically-derived models of sequencing errors

NGmerge: Merging paired-end reads via novel empirically-derived models of sequencing errors
9    63    0
A sensitive short read homology search tool for paired-end read sequencing data

A sensitive short read homology search tool for paired-end read sequencing data
13    73    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
PVT: An efficient computational procedure to speed up next generation sequence analysis

PVT: An efficient computational procedure to speed up next generation sequence analysis
13    64    0
Báo cáo y học:

Báo cáo y học: "ChIA-PET tool for comprehensive chromatin interaction analysis with paired-end tag sequencing"
1    50    0
Báo cáo y học:

Báo cáo y học: "FusionSeq: a modular framework for finding gene fusions by analyzing paired-end RNA-sequencing data"
19    50    0
Báo cáo y học:

Báo cáo y học: " Identification of fusion genes in breast cancer by paired-end RNA-sequencing"
13    55    0
BWTaligner: a genome short-read aligner

BWTaligner: a genome short-read aligner
5    61    0
Analysis of GC-content in transcriptome sequence of Coscinium Fenestratum (Gaertn.) Colebr Leaf

Analysis of GC-content in transcriptome sequence of Coscinium Fenestratum (Gaertn.) Colebr Leaf
5    80    0
Short paired-end reads trump long singleend reads for expression analysis

Short paired-end reads trump long singleend reads for expression analysis
11    61    0
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
ClonoCalc and ClonoPlot: Immune repertoire analysis from raw files to publication figures with graphical user interface

ClonoCalc and ClonoPlot: Immune repertoire analysis from raw files to publication figures with graphical user interface
6    55    0
GBS-SNP-CROP: A reference-optional pipeline for SNP discovery and plant germplasm characterization using variable length, paired-end genotyping-bysequencing data

GBS-SNP-CROP: A reference-optional pipeline for SNP discovery and plant germplasm characterization using variable length, paired-end genotyping-bysequencing data
15    183    0
Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection

Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection
16    73    0
SeqPurge: Highly-sensitive adapter trimming for paired-end NGS data

SeqPurge: Highly-sensitive adapter trimming for paired-end NGS data
7    71    0
MisFinder: Identify mis-assemblies in an unbiased manner using reference and paired-end reads

MisFinder: Identify mis-assemblies in an unbiased manner using reference and paired-end reads
16    54    0
A long fragment aligner called ALFALFA

A long fragment aligner called ALFALFA
11    67    0
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