"read and understand fairy tales" trang 3 - tải miễn phí từ tailieuXANH
Empirical assessment of the impact of sample number and read depth on RNASeq analysis workflow performance

Empirical assessment of the impact of sample number and read depth on RNASeq analysis workflow performance
12    61    0
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    55    0
Assessing the impact of exact reads on reducing the error rate of read mapping

Assessing the impact of exact reads on reducing the error rate of read mapping
15    154    0
FMLRC: Hybrid long read error correction using an FM-index

FMLRC: Hybrid long read error correction using an FM-index
11    75    0
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    70    0
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
Identification of genome-wide noncanonical spliced regions and analysis of biological functions for spliced sequences using Read-Split-Fly

Identification of genome-wide noncanonical spliced regions and analysis of biological functions for spliced sequences using Read-Split-Fly
12    48    0
A framework for space-efficient read clustering in metagenomic samples

A framework for space-efficient read clustering in metagenomic samples
12    45    0
Meta-aligner: Long-read alignment based on genome statistics

Meta-aligner: Long-read alignment based on genome statistics
9    48    0
LSCplus: A fast solution for improving long read accuracy by short read alignment

LSCplus: A fast solution for improving long read accuracy by short read alignment
9    48    0
An investigation of causes of false positive single nucleotide polymorphisms using simulated reads from a small eukaryote genome

An investigation of causes of false positive single nucleotide polymorphisms using simulated reads from a small eukaryote genome
16    64    0
Improving read mapping using additional prefix grams

Improving read mapping using additional prefix grams
11    52    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
English-they gain practice and reading the news

English-they gain practice and reading the news
116    84    4
Re-examination of two diatom reference genomes using long-read sequencing

Re-examination of two diatom reference genomes using long-read sequencing
25    48    1
Long-read metagenomics retrieves complete single-contig bacterial genomes from canine feces

Long-read metagenomics retrieves complete single-contig bacterial genomes from canine feces
15    69    1
Yes, we can use it: A formal test on the accuracy of low-pass nanopore long-read sequencing for mitophylogenomics and barcoding research using the Caribbean spiny lobster Panulirus argus

Yes, we can use it: A formal test on the accuracy of low-pass nanopore long-read sequencing for mitophylogenomics and barcoding research using the Caribbean spiny lobster Panulirus argus
16    25    1
Illuminating the dark side of the human transcriptome with long read transcript sequencing

Illuminating the dark side of the human transcriptome with long read transcript sequencing
22    74    1
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