Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries. - Test2 - elhamkhani - TriplyDB

Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

http://www.wikidata.org/entity/Q33825803

about

Diversity and community composition of methanogenic archaea in the rumen of Scottish upland sheep assessed by different methods GROM-RD: resolving genomic biases to improve read depth detection of copy number variants Ancient DNA studies: new perspectives on old samples The fast changing landscape of sequencing technologies and their impact on microbial genome assemblies and annotation IVT-seq reveals extreme bias in RNA sequencing Shotgun metagenomes and multiple primer pair-barcode combinations of amplicons reveal biases in metabarcoding analyses of fungi Accurate and comprehensive sequencing of personal genomes Evolutionary Insights into RNA trans-Splicing in Vertebrates Massively parallel sequencing: the new frontier of hematologic genomics Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges Issues and prospects of microRNA-based biomarkers in blood and other body fluids Library construction for next-generation sequencing: overviews and challenges.Viral surveillance and discovery The ability of inner-cell-mass cells to self-renew as embryonic stem cells is acquired following epiblast specification Protein-DNA binding in high-resolution Manipulating microRNAs for improved biomass and biofuels from plant feedstocks Large-scale interaction profiling of PDZ domains through proteomic peptide-phage display using human and viral phage peptidomes Small, smaller, smallest: the origins and evolution of ancient dual symbioses in a Phloem-feeding insect The statistical-mechanics of chromosome conformation capture HCV genotyping from NGS short reads and its application in genotype detection from HCV mixed infected plasma Enhanced Methylation Analysis by Recovery of Unsequenceable Fragments Intrinsic challenges in ancient microbiome reconstruction using 16S rRNA gene amplification Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals Odintifier--A computational method for identifying insertions of organellar origin from modern and ancient high-throughput sequencing data based on haplotype phasing Swabs to genomes: a comprehensive workflow Understanding spatial organizations of chromosomes via statistical analysis of Hi-C data DNA polymerases engineered by directed evolution to incorporate non-standard nucleotides Summarizing and correcting the GC content bias in high-throughput sequencing Admixture and recombination among Toxoplasma gondii lineages explain global genome diversity Translation of 5' leaders is pervasive in genes resistant to eIF2 repression Genome data on the extinct Bison schoetensacki establish it as a sister species of the extant European bison (Bison bonasus)Mapping the regulon of Vibrio cholerae ferric uptake regulator expands its known network of gene regulation.Genome Reduction and Co-evolution between the Primary and Secondary Bacterial Symbionts of Psyllids Future microfluidic and nanofluidic modular platforms for nucleic acid liquid biopsy in precision medicine.Toward reliable biomarker signatures in the age of liquid biopsies - how to standardize the small RNA-Seq workflow Pattern Recognition on Read Positioning in Next Generation Sequencing.Optimized Illumina PCR-free library preparation for bacterial whole genome sequencing and analysis of factors influencing de novo assembly Comparison of DNA Quantification Methods for Next Generation Sequencing.Impact of library preparation protocols and template quantity on the metagenomic reconstruction of a mock microbial community.Active promoters give rise to false positive 'Phantom Peaks' in ChIP-seq experiments.

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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

http://www.wikidata.org/entity/Q33825803

description

2011 nî lūn-bûn

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2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին 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

@zh-hant

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

Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

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type

label

Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

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prefLabel

Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.

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Andreas Gnirke

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Carsten Russ

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Daniel Aird

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David B Jaffe

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Maxwell Danielsson

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Michael G Ross

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Timothy Fennell

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Wei-Sheng Chen

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Genome sequence of the human malaria parasite Plasmodium falciparum

Genome sequencing in microfabricated high-density picolitre reactors

Accurate whole human genome sequencing using reversible terminator chemistry

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

Fast and accurate short read alignment with Burrows-Wheeler transform

A large genome center's improvements to the Illumina sequencing system.

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Real-time DNA sequencing from single polymerase molecules

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