Identification of Substrain-Specific Mutations by Massively Parallel Whole-Genome Resequencing of Synechocystis sp. PCC 6803KANESAKI, Yu; SHIWA, Yuh; TAJIMA, Naoyuki et al.DNA research. 2012, Vol 19, Num 1, pp 67-79, issn 1340-2838, 13 p.Article

Evaluation of cells and biological reagents for adventitious agents using degenerate primer PCR and massively parallel sequencingMCCLENAHAN, Shasta D; UHLENHAUT, Christine; KRAUSE, Philip R et al.Vaccine. 2014, Vol 32, Num 52, pp 7115-7121, issn 0264-410X, 7 p.Article

Challenges of sequencing human genomesKOBOLDT, Daniel C; LI DING; MARDIS, Elaine R et al.Briefings in bioinformatics. 2010, Vol 11, Num 5, pp 484-498, issn 1467-5463, 15 p.Article

A novel method for determining microflora composition using dynamic phylogenetic analysis of 16S ribosomal RNA deep sequencing dataCHAN, Ernest R; HESTER, James; KALADY, Matthew et al.Genomics (San Diego, Calif.). 2011, Vol 98, Num 4, pp 253-259, issn 0888-7543, 7 p.Article

Ensuring the safety of vaccine cell substrates by massively parallel sequencing of the transcriptomeONIONS, D; COTE, C; LOVE, B et al.Vaccine. 2011, Vol 29, Num 41, pp 7117-7121, issn 0264-410X, 5 p.Conference Paper

The ITS region as a target for characterization of fungal communities using emerging sequencing technologiesNILSSON, Rolf Henrik; RYBERG, Martin; ABARENKOV, Kessy et al.FEMS microbiology letters. 2009, Vol 296, Num 1, pp 97-101, issn 0378-1097, 5 p.Article

The Wasp System: An open source environment for managing and analyzing genomic dataMCLELLAN, Andrew S; DUBIN, Robert A; QIANG JING et al.Genomics (San Diego, Calif.). 2012, Vol 100, Num 6, pp 345-351, issn 0888-7543, 7 p.Article

Chloroplast genome sequences from total DNA for plant identificationNOCK, Catherine J; WATERS, Daniel L. E; EDWARDS, Mark A et al.Plant biotechnology journal (Print). 2011, Vol 9, Num 3, pp 328-333, issn 1467-7644, 6 p.Article

Massively Parallel Sequencing for Chromosomal Abnormality Testing in Trophectoderm Cells of Human BlastocystsXUYANG YIN; KE TAN; CHUN GONG et al.Biology of reproduction. 2013, Vol 88, Num 3, issn 0006-3363, 69.1-69.6Article

Genome Analysis of the Domestic Dog (Korean Jindo) by Massively Parallel SequencingRYONG NAM KIM; KIM, Dae-Soo; FUJIYAMA, Asao et al.DNA research. 2012, Vol 19, Num 3, pp 275-287, issn 1340-2838, 13 p.Article

Characterizing homologues of crop domestication genes in poorly described wild relatives by high-throughput sequencing of whole genomesMALORY, Sylvia; SHAPTER, Frances M; ELPHINSTONE, Martin S et al.Plant biotechnology journal (Print). 2011, Vol 9, Num 9, pp 1131-1140, issn 1467-7644, 10 p.Article

In-depth analysis of G-to-A hypermutation rate in HIV-1 env DNA induced by endogenous APOBEC3 proteins using massively parallel sequencingKNOEPFEL, Stefanie A; DI GIALLONARDO, Francesca; DÄUMER, Martin et al.Journal of virological methods. 2011, Vol 171, Num 2, pp 329-338, issn 0166-0934, 10 p.Article

Distinguishing Hyperglycemic Changes by Set7 in Vascular Endothelial CellsOKABE, Jun; ORLOWSKI, Christian; BALCERCZYK, Aneta et al.Circulation research. 2012, Vol 110, Num 8, pp 1067-1076, issn 0009-7330, 10 p.Article

Identification of Novel FMR1 Variants by Massively Parallel Sequencing in Developmentally Delayed MalesCOLLINS, Stephen C; BRAY, Steven M; SUHL, Joshua A et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 10, pp 2512-2520, issn 1552-4825, 9 p.Article

Recent advances in the analysis of fetal nucleic acids in maternal plasmaNANCY BO YIN TSUI; YUK MING DENNIS LO.Current opinion in hematology. 2012, Vol 19, Num 6, pp 462-468, issn 1065-6251, 7 p.Article

Targeted next generation sequencing as a diagnostic tool in epileptic disordersLEMKE, Johannes R; RIESCH, Erik; STROZZI, Susi et al.Epilepsia (Copenhagen). 2012, Vol 53, Num 8, pp 1387-1398, issn 0013-9580, 12 p.Article

From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancerLAPUK, Anna V; CHUNXIAO WU; HAEGERT, Anne et al.Journal of pathology (Print). 2012, Vol 227, Num 3, pp 286-297, issn 0022-3417, 12 p.Article

Capturing intra-tumor genetic heterogeneity by de novo mutation profiling of circulating cell-free tumor DNA: a proof-of-principleDE MATTOS-ARRUDA, L; WEIGELT, B; PISCUOGLIO, S et al.Annals of oncology. 2014, Vol 25, Num 9, pp 1729-1735, issn 0923-7534, 7 p.Article

FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancerPARK, Daniel J; ODEFREY, Fabrice A; SINILNIKOVA, Olga M et al.Breast cancer research and treatment. 2011, Vol 130, Num 3, pp 1043-1049, issn 0167-6806, 7 p.Article

Low-coverage massively parallel pyrosequencing of cDNAs enables proteomics in non-model species : Comparison of a species-specific database generated by pyrosequencing with databases from related species for proteome analysis of pea chloroplast envelopesBRÄUTIGAM, Andrea; SHRESTHA, Roshan P; WHITTEN, Doug et al.Journal of biotechnology. 2008, Vol 136, Num 1-2, pp 44-53, issn 0168-1656, 10 p.Article

Networking: a community approach to invaders and their parasites : INVASIONS AND INFECTIONSROY, Helen E; LAWSON HANDLEY, Lori-Jayne.Functional ecology (Print). 2012, Vol 26, Num 6, pp 1238-1248, issn 0269-8463, 11 p.Article

Sensitive and specific detection of EML4-ALK rearrangements in non-small cell lung cancer (NSCLC) specimens by multiplex amplicon RNA massive parallel sequencingMOSKALEV, Evgeny A; FROHNAUER, Judith; RIEKER, Ralf J et al.Lung cancer. 2014, Vol 84, Num 3, pp 215-221, issn 0169-5002, 7 p.Article

Detection of BCR-ABL1 mutations in chronic myeloid leukaemia by massive parallel sequencingEYAL, Eran; TOHAMI, Tali; AMIR, Amnon et al.British journal of haematology. 2013, Vol 160, Num 4, pp 477-486, issn 0007-1048, 10 p.Article

Network- and Attribute-Based Classifiers can Prioritize Genes and Pathways for Autism Spectrum Disorders and Intellectual DisabilityYAN KOU; BETANCUR, Catalina; HUILEI XU et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2012, Vol 160, Num 2, pp 130-142, issn 1552-4868, 13 p.Article

Recessive RYR1 Mutations in a Patient With Severe Congenital Nemaline Myopathy With Ophthalomoplegia Identified Through Massively Parallel SequencingKONDO, Eri; NISHIMURA, Takafumi; FURUKAWA, Toru et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 4, pp 772-778, issn 1552-4825, 7 p.Article