"Next generation mapping" trang 1 - tải miễn phí từ tailieunhanh
SNVHMM: Predicting single nucleotide variants from next generation sequencing

SNVHMM: Predicting single nucleotide variants from next generation sequencing
11    34    1
Rapid fine mapping of causative mutations from sets of unordered, contig-sized fragments of genome sequence

Rapid fine mapping of causative mutations from sets of unordered, contig-sized fragments of genome sequence
7    58    1
Adaptable probabilistic mapping of short reads using position specific scoring matrices

Adaptable probabilistic mapping of short reads using position specific scoring matrices
17    62    1
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    39    1
Fast and efficient short read mapping based on a succinct hash index

Fast and efficient short read mapping based on a succinct hash index
14    53    1
Benchmarking short sequence mapping tools

Benchmarking short sequence mapping tools
25    53    1
Construction of a high-density genetic map and QTLs mapping for sugars and acids in grape berries

Construction of a high-density genetic map and QTLs mapping for sugars and acids in grape berries
14    82    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    53    1
Improving read mapping using additional prefix grams

Improving read mapping using additional prefix grams
11    31    1
First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data

First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data
13    57    1
Novel read density distribution score shows possible aligner artefacts, when mapping a single chromosome

Novel read density distribution score shows possible aligner artefacts, when mapping a single chromosome
11    37    1
Detailed evaluation of cancer sequencing pipelines in different microenvironments and heterogeneity levels

Detailed evaluation of cancer sequencing pipelines in different microenvironments and heterogeneity levels
13    53    1
ARKS: Chromosome-scale scaffolding of human genome drafts with linked read kmers

ARKS: Chromosome-scale scaffolding of human genome drafts with linked read kmers
10    41    1
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    35    1