"High throughput next generation sequencing" trang 1 - tải miễn phí từ tailieunhanh
High-throughput next-generation sequencing for identifying pathogens during early-stage post-lung transplantation

High-throughput next-generation sequencing for identifying pathogens during early-stage post-lung transplantation
9    40    1
Quantification of experimentally induced nucleotide conversions in high-throughput sequencing datasets

Quantification of experimentally induced nucleotide conversions in high-throughput sequencing datasets
16    52    1
ANGSD: Analysis of next generation sequencing data

ANGSD: Analysis of next generation sequencing data
13    61    1
Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing

Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing
8    36    1
Modeling the next generation sequencing sample processing pipeline for the purposes of classification

Modeling the next generation sequencing sample processing pipeline for the purposes of classification
14    24    1
Fluorescent amplification for next generation sequencing (FA-NGS) library preparation

Fluorescent amplification for next generation sequencing (FA-NGS) library preparation
9    26    2
Robust Sub-nanomolar Library Preparation for High Throughput Next Generation Sequencing

Robust Sub-nanomolar Library Preparation for High Throughput Next Generation Sequencing
10    25    1
A T-DNA mutant screen that combines high-throughput phenotyping with the efficient identification of mutated genes by targeted genome sequencing

A T-DNA mutant screen that combines high-throughput phenotyping with the efficient identification of mutated genes by targeted genome sequencing
12    108    0
Enrichment post-library preparation enhances the sensitivity of highthroughput sequencing-based detection and characterization of viruses from complex samples

Enrichment post-library preparation enhances the sensitivity of highthroughput sequencing-based detection and characterization of viruses from complex samples
14    44    1
QTrim: A novel tool for the quality trimming of sequence reads generated using the Roche/454 sequencing platform

QTrim: A novel tool for the quality trimming of sequence reads generated using the Roche/454 sequencing platform
6    34    1
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    62    1
NEAT: A framework for building fully automated NGS pipelines and analyses

NEAT: A framework for building fully automated NGS pipelines and analyses
9    84    1
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    53    1
Evaluation of variant detection software for pooled next-generation sequence data

Evaluation of variant detection software for pooled next-generation sequence data
9    31    1
Error correction and statistical analyses for intra-host comparisons of feline immunodeficiency virus diversity from high-throughput sequencing data

Error correction and statistical analyses for intra-host comparisons of feline immunodeficiency virus diversity from high-throughput sequencing data
14    56    1
Reference-free compression of high throughput sequencing data with a probabilistic de Bruijn graph

Reference-free compression of high throughput sequencing data with a probabilistic de Bruijn graph
14    40    1
ShatterProof: Operational detection and quantification of chromothripsis

ShatterProof: Operational detection and quantification of chromothripsis
13    38    1
A high throughput screen for active human transposable elements

A high throughput screen for active human transposable elements
14    31    1
CODEX2: Full-spectrum copy number variation detection by high-throughput DNA sequencing

CODEX2: Full-spectrum copy number variation detection by high-throughput DNA sequencing
13    20    1
VISPA2: A scalable pipeline for highthroughput identification and annotation of vector integration sites

VISPA2: A scalable pipeline for highthroughput identification and annotation of vector integration sites
12    56    1