"Read data" trang 1 - tải miễn phí từ tailieuXANH
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
Detecting large deletions at base pair level by combining split read and paired read data

Detecting large deletions at base pair level by combining split read and paired read data
7    45    0
Opportunities and challenges in long-read sequencing data analysis

Opportunities and challenges in long-read sequencing data analysis
16    129    1
NextSV: A meta-caller for structural variants from low-coverage long-read sequencing data

NextSV: A meta-caller for structural variants from low-coverage long-read sequencing data
11    64    0
HISEA: HIerarchical SEed Aligner for PacBio data

HISEA: HIerarchical SEed Aligner for PacBio data
13    40    0
SInC: An accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence data

SInC: An accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence data
9    42    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
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    1
A graphical, interactive and GPU-enabled workflow to process long-read sequencing data

A graphical, interactive and GPU-enabled workflow to process long-read sequencing data
8    233    1
HAPDeNovo: A haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data

HAPDeNovo: A haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data
7    140    1
Comprehensive characterization of singlecell full-length isoforms in human and mouse with long-read sequencing

Comprehensive characterization of singlecell full-length isoforms in human and mouse with long-read sequencing
24    223    1
The Lair: a resource for exploratory analysis of published RNA-Seq data

The Lair: a resource for exploratory analysis of published RNA-Seq data
6    62    0
Impact of data resolution on three-dimensional structure inference methods

Impact of data resolution on three-dimensional structure inference methods
13    90    0
ATRAM - automated target restricted assembly method: A fast method for assembling loci across divergent taxa from next-generation sequencing data

ATRAM - automated target restricted assembly method: A fast method for assembling loci across divergent taxa from next-generation sequencing data
7    68    0
NanoMod: A computational tool to detect DNA modifications using Nanopore longread sequencing data

NanoMod: A computational tool to detect DNA modifications using Nanopore longread sequencing data
12    69    1
ExpansionHunter Denovo: A computational method for locating known and novel repeat expansions in short-read sequencing data

ExpansionHunter Denovo: A computational method for locating known and novel repeat expansions in short-read sequencing data
14    243    1
Báo cáo y học:

Báo cáo y học: "Modeling non-uniformity in short-read rates in RNA-Seq data"
1    41    0
Báo cáo y học:

Báo cáo y học: "Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA"
12    54    0
Báo cáo y học:

Báo cáo y học: " PARalyzer: definition of RNA binding sites from PAR-CLIP short-read sequence data"
16    51    0
Bài giảng Lập trình NET và C#: Lecture 14 - TS Đào Nam Anh

Bài giảng Lập trình NET và C#: Lecture 14 - TS Đào Nam Anh
8    42    0
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