Sequence-specific error profile of Illumina sequencers. - Wikidata - wikimedia - TriplyDB

Sequence-specific error profile of Illumina sequencers.

Sequence-specific error profile of Illumina sequencers.

http://www.wikidata.org/entity/Q34185285

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Characterization of uncultivable bat influenza virus using a replicative synthetic virus Metagenomics - a guide from sampling to data analysis A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers.IVT-seq reveals extreme bias in RNA sequencing Metagenomics for pathogen detection in public health Next Generation Sequencing of Actinobacteria for the Discovery of Novel Natural Products Metagenomics: Retrospect and Prospects in High Throughput Age Resistance of Hepatitis C Virus to Inhibitors: Complexity and Clinical Implications Next-generation sequencing in clinical virology: Discovery of new viruses Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges Quantifying influenza virus diversity and transmission in humans.IPED: a highly efficient denoising tool for Illumina MiSeq Paired-end 16S rRNA gene amplicon sequencing data Adaptable probabilistic mapping of short reads using position specific scoring matrices.Advantages of Array-Based Technologies for Pre-Emptive Pharmacogenomics Testing High-throughput RNA sequencing of a formalin-fixed, paraffin-embedded autopsy lung tissue sample from the 1918 influenza pandemic The soft palate is an important site of adaptation for transmissible influenza viruses Within Host Evolution Selects for a Dominant Genotype of Mycobacterium tuberculosis while T Cells Increase Pathogen Genetic Diversity Guanine holes are prominent targets for mutation in cancer and inherited disease Development of synchronous VHL syndrome tumors reveals contingencies and constraints to tumor evolution Estimation of sequencing error rates in short reads Challenges and opportunities in estimating viral genetic diversity from next-generation sequencing data Summarizing and correcting the GC content bias in high-throughput sequencing Comparative RNA sequencing reveals substantial genetic variation in endangered primates Toward reliable biomarker signatures in the age of liquid biopsies - how to standardize the small RNA-Seq workflow Illumina MiSeq sequencing disfavours a sequence motif in the GFP reporter gene.Evaluation of Nine Somatic Variant Callers for Detection of Somatic Mutations in Exome and Targeted Deep Sequencing Data.Presence of oseltamivir-resistant pandemic A/H1N1 minor variants before drug therapy with subsequent selection and transmission.Viral population analysis and minority-variant detection using short read next-generation sequencing.An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data Characterizing and measuring bias in sequence data.Cell periphery-related proteins as major genomic targets behind the adaptive evolution of an industrial Saccharomyces cerevisiae strain to combined heat and hydrolysate stress Coval: improving alignment quality and variant calling accuracy for next-generation sequencing data.Estimating genotype error rates from high-coverage next-generation sequence data.Detecting non-allelic homologous recombination from high-throughput sequencing data.Distinguishing low frequency mutations from RT-PCR and sequence errors in viral deep sequencing data.Underlying Data for Sequencing the Mitochondrial Genome with the Massively Parallel Sequencing Platform Ion Torrent™ PGM™PathoQC: Computationally Efficient Read Preprocessing and Quality Control for High-Throughput Sequencing Data Sets.Genotype-Frequency Estimation from High-Throughput Sequencing Data.Intra-individual polymorphism in chloroplasts from NGS data: where does it come from and how to handle it?Choice of reference-guided sequence assembler and SNP caller for analysis of Listeria monocytogenes short-read sequence data greatly influences rates of error.

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Sequence-specific error profile of Illumina sequencers.

http://www.wikidata.org/entity/Q34185285

description

2011 nî lūn-bûn

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2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2011 թվականի մայիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Sequence-specific error profile of Illumina sequencers.

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Sequence-specific error profile of Illumina sequencers.

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Sequence-specific error profile of Illumina sequencers.

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type

label

Sequence-specific error profile of Illumina sequencers.

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Sequence-specific error profile of Illumina sequencers.

@en

Sequence-specific error profile of Illumina sequencers.

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prefLabel

Sequence-specific error profile of Illumina sequencers.

@ast

Sequence-specific error profile of Illumina sequencers.

@en

Sequence-specific error profile of Illumina sequencers.

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Nucleic Acids Research

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Sequence-specific error profile of Illumina sequencers.

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Aki Hirai

http://www.w3.org/2001/XMLSchema#string

Hirofumi Yoshikawa

http://www.w3.org/2001/XMLSchema#string

Hiroki Takahashi

http://www.w3.org/2001/XMLSchema#string

Kensuke Nakamura

http://www.w3.org/2001/XMLSchema#string

Margaret C Linak

http://www.w3.org/2001/XMLSchema#string

Md Altaf-Ul-Amin

http://www.w3.org/2001/XMLSchema#string

Naotake Ogasawara

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Shigehiko Kanaya

http://www.w3.org/2001/XMLSchema#string

Shun Ikeda

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Taku Oshima

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P2860

BFAST: an alignment tool for large scale genome resequencing

De novo genome sequence assembly of a filamentous fungus using Sanger, 454 and Illumina sequence data

Unlocking short read sequencing for metagenomics

SHRiMP: accurate mapping of short color-space reads

Fast mapping of short sequences with mismatches, insertions and deletions using index structures

The sequence and de novo assembly of the giant panda genome

Genome sequencing in microfabricated high-density picolitre reactors

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

RNA-Seq: a revolutionary tool for transcriptomics

The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants

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10.1093/NAR/GKR344

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13

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39

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2011-05-16T00:00:00Z

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