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DNA sequencing artifacts : band smearing and lossLI DAO KE; RAJESHWAR RAO-TEKMAL; SHAIN, S. A et al.BioTechniques. 1993, Vol 15, Num 5, issn 0736-6205, p. 840Article

Development of a Dual-Index Sequencing Strategy and Curation Pipeline for Analyzing Amplicon Sequence Data on the MiSeq Illumina Sequencing PlatformKOZICH, James J; WESTCOTT, Sarah L; BAXTER, Nielson T et al.Applied and environmental microbiology (Print). 2013, Vol 79, Num 17, pp 5112-5120, issn 0099-2240, 9 p.Article

ART: a next-generation sequencing read simulatorWEICHUN HUANG; LEPING LI; MYERS, Jason R et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 4, pp 593-594, issn 1367-4803, 2 p.Article

Landscape of Next-Generation Sequencing Technologies : FUNDAMENTAL AND APPLIED REVIEWS IN ANALYTICAL CHEMISTRYNIEDRINGHAUS, Thomas P; MILANOVA, Denitsa; KERBY, Matthew B et al.Analytical chemistry (Washington). 2011, Vol 83, Num 12, pp 4327-4341, issn 0003-2700, 15 p.Article

Next generation deep sequencing and vaccine design: today and tomorrowLUCIANI, Fabio; BULL, Rowena A; LLOYD, Andrew R et al.Trends in biotechnology (Regular ed.). 2012, Vol 30, Num 9, pp 443-452, issn 0167-7799, 10 p.Article

Isolement de Bordetella trematum au décours d'une bactériémie = Isolation of Bordetella trematum from bacteremiaHALIM, Ilham; IHBIBANE, Fatima; BELABBES, Houria et al.Annales de biologie clinique (Paris). 2014, Vol 72, Num 5, pp 612-614, issn 0003-3898, 3 p.Article

GRASS: a generic algorithm for scaffolding next-generation sequencing assembliesGRITSENKO, Alexey A; NIJKAMP, Jurgen F; REINDERS, Marcel J. T et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 11, pp 1429-1437, issn 1367-4803, 9 p.Article

Qualimap: evaluating next-generation sequencing alignment dataGARCIA-ALCALDE, Fernando; OKONECHNIKOV, Konstantin; CARBONELL, Jose et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 20, pp 2678-2679, issn 1367-4803, 2 p.Article

Bambino: a variant detector and alignment viewer for next-generation sequencing data in the SAM/BAM formatEDMONSON, Michael N; JINGHUI ZHANG; CHUNHUA YAN et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 6, pp 865-866, issn 1367-4803, 2 p.Article

Revisiting Mendelian disorders through exome sequencingKU, Chee-Seng; NAIDOO, Nasheen; PAWITAN, Yudi et al.Human genetics. 2011, Vol 129, Num 4, pp 351-370, issn 0340-6717, 20 p.Article

Blocking oligonucleotides improve sequencing through inverted repeatsESPOSITO, Dominic; GILLETTE, William K; HARTLEY, James L et al.BioTechniques. 2003, Vol 35, Num 5, pp 914-920, issn 0736-6205, 4 p.Article

BAC end sequencing: A standard in the genomics tools repertoireHITTI, Joseph; BARBAGALLO, Christopher A.American biotechnology laboratory. 2003, Vol 21, Num 11, pp 48-49, issn 0749-3223, 2 p.Article

Caractérisation d'un allergène de Schistosoma mansoni = Characterization of a Schistosoma mansonii allergenBoutin, Philippe; Capron, André.1990, 97 p.Thesis

The expanding scope of DNA sequencingSHENDURE, Jay; LIEBERMAN AIDEN, Erez.Nature biotechnology (Print). 2012, Vol 30, Num 11, pp 1084-1094, issn 1087-0156, 11 p.Article

Séquençage de nouvelle génération: déjà en clinique? = Is NGS cilready in clinical use?JORDAN, Bertrand.MS. Médecine sciences. 2011, Vol 27, Num 12, pp 1127-1130, issn 0767-0974, 4 p.Article

Sequencing's new racePODOLAK, Erin.BioTechniques. 2010, Vol 48, Num 2, issn 0736-6205, 105-111 [4 p.]Article

girafe ― an R/Bioconductor package for functional exploration of aligned next-generation sequencing readsTOEDLING, Joern; CIAUDO, Constance; VOINNET, Olivier et al.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 22, pp 2902-2903, issn 1367-4803, 2 p.Article

A window into third-generation sequencingSCHADT, Eric E; TURNER, Steve; KASARSKIS, Andrew et al.Human molecular genetics (Print). 2010, Vol 19, issn 0964-6906, R227-R240, NS2Article

Hadoop-BAM: directly manipulating next generation sequencing data in the cloudNIEMENMAA, Matti; KALLIO, Aleksi; SCHUMACHER, Andre et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 6, pp 876-877, issn 1367-4803, 2 p.Article

A framework for variation discovery and genotyping using next-generation DNA sequencing dataDEPRISTO, Mark A; BANKS, Eric; MCKENNA, Aaron et al.Nature genetics. 2011, Vol 43, Num 5, pp 491-498, issn 1061-4036, 8 p.Article

Exome sequencing identifies the cause of a mendelian disorderNG, Sarah B; BUCKINGHAM, Kati J; SHENDURE, Jay et al.Nature genetics. 2010, Vol 42, Num 1, pp 30-35, issn 1061-4036, 6 p.Article

Extremely low-coverage sequencing and imputation increases power for genome-wide association studiesPASANIUC, Bogdan; ROHLAND, Nadin; SULLIVAN, Patrick F et al.Nature genetics. 2012, Vol 44, Num 6, pp 631-635, issn 1061-4036, 5 p.Article

ChimeraScan: a tool for identifying chimeric transcription in sequencing dataLYER, Matthew K; CHINNAIYAN, Arul M; MAHER, Christopher A et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 20, pp 2903-2904, issn 1367-4803, 2 p.Article

SAMStat: monitoring biases in next generation sequencing dataLASSMANN, Timo; HAYASHIZAKI, Yoshihide; DAUB, Carsten O et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 1, pp 130-131, issn 1367-4803, 2 p.Article