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Massively-Parallel Sequencing
Known as:
Next Generation Sequencing
, Next-Generation Sequencing
, Massively Parallel DNA Sequencing
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Technologies that facilitate the rapid determination of the DNA sequence of large numbers of strands or segments of DNA.
National Institutes of Health
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Related topics
Related topics
2 relations
Clinical Data Interchange Standards Consortium Terminology
Broader (1)
High-Throughput Nucleotide Sequencing
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2020
Highly Cited
2020
Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China
Chaolin Huang
,
Ye-ming Wang
,
+26 authors
B. Cao
The Lancet
2020
Corpus ID: 210886197
Highly Cited
2020
Highly Cited
2020
A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster
J. Chan
,
Shuofeng Yuan
,
+18 authors
K. Yuen
The Lancet
2020
Corpus ID: 210886211
Highly Cited
2015
Highly Cited
2015
Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular…
Sue Richards
,
Nazneen Aziz
,
+9 authors
H. Rehm
Genetics in Medicine
2015
Corpus ID: 52873669
Disclaimer: These ACMG Standards and Guidelines were developed primarily as an educational resource for clinical laboratory…
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Highly Cited
2014
Highly Cited
2014
Trimmomatic: a flexible trimmer for Illumina sequence data
Anthony M. Bolger
,
M. Lohse
,
B. Usadel
Bioinform.
2014
Corpus ID: 7324039
Motivation: Although many next-generation sequencing (NGS) read preprocessing tools already existed, we could not find any tool…
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Highly Cited
2012
Highly Cited
2012
Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration
H. Thorvaldsdóttir
,
James T. Robinson
,
J. Mesirov
Briefings Bioinform.
2012
Corpus ID: 3444507
Data visualization is an essential component of genomic data analysis. However, the size and diversity of the data sets produced…
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Highly Cited
2011
Highly Cited
2011
A framework for variation discovery and genotyping using next-generation DNA sequencing data
M. DePristo
,
E. Banks
,
+15 authors
M. Daly
Nature Genetics
2011
Corpus ID: 18263665
Recent advances in sequencing technology make it possible to comprehensively catalog genetic variation in population samples…
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Highly Cited
2011
Highly Cited
2011
FLASH: fast length adjustment of short reads to improve genome assemblies
Tanja Magoc
,
S. Salzberg
Bioinform.
2011
Corpus ID: 11906282
MOTIVATION Next-generation sequencing technologies generate very large numbers of short reads. Even with very deep genome…
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Review
2010
Review
2010
Sequencing technologies — the next generation
M. Metzker
Nature reviews genetics
2010
Corpus ID: 205484500
Demand has never been greater for revolutionary technologies that deliver fast, inexpensive and accurate genome information. This…
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Highly Cited
2009
Highly Cited
2009
Targeted capture and massively parallel sequencing of 12 human exomes
Sarah Ng
,
Emily H Turner
,
+10 authors
J. Shendure
2009
Corpus ID: 26586878
Genome-wide association studies suggest that common genetic variants explain only a modest fraction of heritable risk for common…
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Highly Cited
2008
Highly Cited
2008
The complete genome of an individual by massively parallel DNA sequencing
D. Wheeler
,
Maithreyan Srinivasan
,
+24 authors
J. Rothberg
Nature
2008
Corpus ID: 4429736
The association of genetic variation with disease and drug response, and improvements in nucleic acid technologies, have given…
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