Substantial biases in ultra-short read data sets from high-throughput DNA sequencing - Wikidata - wikimedia - TriplyDB

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

http://www.wikidata.org/entity/Q29617050

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Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysis The first symbiont-free genome sequence of marine red alga, Susabi-nori (Pyropia yezoensis)Genome-wide chromatin remodeling identified at GC-rich long nucleosome-free regions ConDeTri--a content dependent read trimmer for Illumina data Weakly positioned nucleosomes enhance the transcriptional competency of chromatin A complete mitochondrial genome sequence from a mesolithic wild aurochs (Bos primigenius)Optimizing hybrid assembly of next-generation sequence data from Enterococcus faecium: a microbe with highly divergent genome Comparative and joint analysis of two metagenomic datasets from a biogas fermenter obtained by 454-pyrosequencing Fast mapping of short sequences with mismatches, insertions and deletions using index structures IVT-seq reveals extreme bias in RNA sequencing A Draft Sequence of the Neandertal Genome Gene prediction with Glimmer for metagenomic sequences augmented by classification and clustering Biases in Illumina transcriptome sequencing caused by random hexamer priming SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood Best practices for evaluating single nucleotide variant calling methods for microbial genomics A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome Using familial information for variant filtering in high-throughput sequencing studies Viral surveillance and discovery New virologic tools for management of chronic hepatitis B and C Host-Microbiome Interaction and Cancer: Potential Application in Precision Medicine Advantages of Array-Based Technologies for Pre-Emptive Pharmacogenomics Testing Hybrid error correction and de novo assembly of single-molecule sequencing reads ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia The statistical-mechanics of chromosome conformation capture Ultra-fast local-haplotype variant calling using paired-end DNA-sequencing data reveals somatic mosaicism in tumor and normal blood samples Reference-free validation of short read data HCV genotyping from NGS short reads and its application in genotype detection from HCV mixed infected plasma Purifying Selection Maintains Dosage-Sensitive Genes during Degeneration of the Threespine Stickleback Y Chromosome Differential and coherent processing patterns from small RNAs High-throughput sequencing technologies Comparative transcriptome of wild type and selected strains of the microalgae Tisochrysis lutea provides insights into the genetic basis, lipid metabolism and the life cycle Single Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) Data The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation Probabilistic error correction for RNA sequencing Evaluation of genome sequencing quality in selected plant species using expressed sequence tags 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

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Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

http://www.wikidata.org/entity/Q29617050

description

2008 nî lūn-bûn

@nan

2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

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2008年論文

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2008年论文

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name

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

@ast

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

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type

label

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

@ast

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

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prefLabel

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

@ast

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

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Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

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Borodina T

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Dohm JC

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Himmelbauer H

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Lottaz C

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P2860

DNA sequencing with chain-terminating inhibitors

Genome sequencing in microfabricated high-density picolitre reactors

SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing

An analysis of the feasibility of short read sequencing

High-resolution profiling of histone methylations in the human genome

Who ate whom? Adaptive Helicobacter genomic changes that accompanied a host jump from early humans to large felines

Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning

Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing

Specific enzymatic amplification of DNA in vitro: the polymerase chain reaction

Accuracy and quality of massively parallel DNA pyrosequencing.

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10.1093/NAR/GKN425

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