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Refinado por: assunto: High-Throughput Nucleotide Sequencing - Methods remover
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KRAS/GNAS‐testing by highly sensitive deep targeted next generation sequencing improves the endoscopic ultrasound‐guided workup of suspected mucinous neoplasms of the pancreas
KRAS/GNAS‐testing by highly sensitive deep targeted next generation sequencing improves the endoscopic ultrasound‐guided workup of suspected mucinous neoplasms of the pancreas
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KRAS/GNAS‐testing by highly sensitive deep targeted next generation sequencing improves the endoscopic ultrasound‐guided workup of suspected mucinous neoplasms of the pancreas

Schmitz, Daniel ; Kazdal, Daniel ; Allgäuer, Michael ; Trunk, Marcus ; Vornhusen, Sylke ; Nahm, Anna‐Maria ; Doll, Matthias ; Weingärtner, Simon ; Endris, Volker ; Penzel, Roland ; Kirchner, Martina ; Brandt, Regine ; Neumann, Olaf ; Sültmann, Holger ; Budczies, Jan ; Kienle, Peter ; Magdeburg, Richard ; Hetjens, Svetlana ; Schirmacher, Peter ; Bergmann, Frank ; Rudi, Jochen ; Stenzinger, Albrecht ; Volckmar, Anna‐Lena

Genes chromosomes & cancer, 2021-07, Vol.60 (7), p.489-497 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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2
Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms
Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms
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Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms

Caporaso, J Gregory ; Lauber, Christian L ; Walters, William A ; Berg-Lyons, Donna ; Huntley, James ; Fierer, Noah ; Owens, Sarah M ; Betley, Jason ; Fraser, Louise ; Bauer, Markus ; Gormley, Niall ; Gilbert, Jack A ; Smith, Geoff ; Knight, Rob

The ISME Journal, 2012-08, Vol.6 (8), p.1621-1624 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Seq-Well: portable, low-cost RNA sequencing of single cells at high throughput
Seq-Well: portable, low-cost RNA sequencing of single cells at high throughput
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Seq-Well: portable, low-cost RNA sequencing of single cells at high throughput

Gierahn, Todd M ; Wadsworth, 2nd, Marc H ; Hughes, Travis K ; Bryson, Bryan D ; Butler, Andrew ; Satija, Rahul ; Fortune, Sarah ; Love, J Christopher ; Shalek, Alex K

Nature methods, 2017-04, Vol.14 (4), p.395-398 [Periódico revisado por pares]

United States: Nature Publishing Group

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4
The Next-Generation Sequencing Revolution and Its Impact on Genomics
The Next-Generation Sequencing Revolution and Its Impact on Genomics
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The Next-Generation Sequencing Revolution and Its Impact on Genomics

Koboldt, Daniel C. ; Steinberg, Karyn Meltz ; Larson, David E. ; Wilson, Richard K. ; Mardis, Elaine R.

Cell, 2013-09, Vol.155 (1), p.27-38 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next‐generation sequencing with a 25‐gene panel
Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next‐generation sequencing with a 25‐gene panel
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Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next‐generation sequencing with a 25‐gene panel

Tung, Nadine ; Battelli, Chiara ; Allen, Brian ; Kaldate, Rajesh ; Bhatnagar, Satish ; Bowles, Karla ; Timms, Kirsten ; Garber, Judy E. ; Herold, Christina ; Ellisen, Leif ; Krejdovsky, Jill ; DeLeonardis, Kim ; Sedgwick, Kristin ; Soltis, Kathleen ; Roa, Benjamin ; Wenstrup, Richard J. ; Hartman, Anne‐Renee

Cancer, 2015-01, Vol.121 (1), p.25-33 [Periódico revisado por pares]

United States

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6
Making the Leap from Research Laboratory to Clinic: Challenges and Opportunities for Next-Generation Sequencing in Infectious Disease Diagnostics
Making the Leap from Research Laboratory to Clinic: Challenges and Opportunities for Next-Generation Sequencing in Infectious Disease Diagnostics
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Making the Leap from Research Laboratory to Clinic: Challenges and Opportunities for Next-Generation Sequencing in Infectious Disease Diagnostics

Goldberg, Brittany ; Sichtig, Heike ; Geyer, Chelsie ; Ledeboer, Nathan ; Weinstock, George M

mBio, 2015-12, Vol.6 (6), p.e01888-e01815 [Periódico revisado por pares]

United States: American Society of Microbiology

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7
Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and genome analyzer systems
Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and genome analyzer systems
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Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and genome analyzer systems

Minoche, André E ; Dohm, Juliane C ; Himmelbauer, Heinz

Genome biology, 2011-11, Vol.12 (11), p.R112-R112 [Periódico revisado por pares]

England: BioMed Central

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8
Cost-effectiveness analyses of genetic and genomic diagnostic tests
Cost-effectiveness analyses of genetic and genomic diagnostic tests
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Cost-effectiveness analyses of genetic and genomic diagnostic tests

Payne, Katherine ; Gavan, Sean P ; Wright, Stuart J ; Thompson, Alexander J

Nature reviews. Genetics, 2018-04, Vol.19 (4), p.235-246 [Periódico revisado por pares]

England: Nature Publishing Group

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9
Systematic comparison of germline variant calling pipelines cross multiple next-generation sequencers
Systematic comparison of germline variant calling pipelines cross multiple next-generation sequencers
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Systematic comparison of germline variant calling pipelines cross multiple next-generation sequencers

Chen, Jiayun ; Li, Xingsong ; Zhong, Hongbin ; Meng, Yuhuan ; Du, Hongli

Scientific reports, 2019-06, Vol.9 (1), p.9345-13, Article 9345 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants
Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants
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Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants

Beck, Tyler F ; Mullikin, James C ; Biesecker, Leslie G

Clinical chemistry (Baltimore, Md.), 2016-04, Vol.62 (4), p.647-654 [Periódico revisado por pares]

England: American Association for Clinical Chemistry, Inc

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