about
ConDeTri--a content dependent read trimmer for Illumina dataThree-stage quality control strategies for DNA re-sequencing dataProspects and limitations of full-text index structures in genome analysisReference-free validation of short read dataProbabilistic error correction for RNA sequencingEstimation of sequencing error rates in short readsOptimized Illumina PCR-free library preparation for bacterial whole genome sequencing and analysis of factors influencing de novo assemblyA bioinformatician's guide to the forefront of suffix array construction algorithmsMusket: a multistage k-mer spectrum-based error corrector for Illumina sequence data.PRICE: software for the targeted assembly of components of (Meta) genomic sequence dataDRISEE overestimates errors in metagenomic sequencing data.Next-generation sequence assembly: four stages of data processing and computational challengesOligotyping: Differentiating between closely related microbial taxa using 16S rRNA gene data.Correcting Illumina data.Karect: accurate correction of substitution, insertion and deletion errors for next-generation sequencing data.CRCDA--Comprehensive resources for cancer NGS data analysis.RecountDB: a database of mapped and count corrected transcribed sequences.ADEPT, a dynamic next generation sequencing data error-detection program with trimming.A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysis.From next-generation resequencing reads to a high-quality variant data set.MapReduce for accurate error correction of next-generation sequencing data.Correction of sequencing errors in a mixed set of reads.HECTOR: a parallel multistage homopolymer spectrum based error corrector for 454 sequencing data.HiTEC: accurate error correction in high-throughput sequencing data.Overcoming bias and systematic errors in next generation sequencing dataRepeat-aware modeling and correction of short read errors.Querying large read collections in main memory: a versatile data structure.Error correction of high-throughput sequencing datasets with non-uniform coverage.Slim-filter: an interactive Windows-based application for illumina genome analyzer data assessment and manipulation.BLESS: bloom filter-based error correction solution for high-throughput sequencing reads.Blue: correcting sequencing errors using consensus and context.Denoising DNA deep sequencing data-high-throughput sequencing errors and their correction.Lighter: fast and memory-efficient sequencing error correction without counting.Benchmarking short sequence mapping toolsSequencing error correction without a reference genome.ECHO: a reference-free short-read error correction algorithm.Quake: quality-aware detection and correction of sequencing errorsFiona: a parallel and automatic strategy for read error correction.ACE: accurate correction of errors using K-mer tries.Indexing Arbitrary-Length k-Mers in Sequencing Reads.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
SHREC: a short-read error correction method.
@ast
SHREC: a short-read error correction method.
@en
type
label
SHREC: a short-read error correction method.
@ast
SHREC: a short-read error correction method.
@en
prefLabel
SHREC: a short-read error correction method.
@ast
SHREC: a short-read error correction method.
@en
P2093
P356
P1433
P1476
SHREC: a short-read error correction method.
@en
P2093
Bertil Schmidt
Heiko Schröder
Jan Schröder
Ranjan Sinha
Simon J Puglisi
P304
P356
10.1093/BIOINFORMATICS/BTP379
P407
P577
2009-06-19T00:00:00Z