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Biopolymer Sequencing
Known as:
SEQUENCING
A process to identify and determine the primary structure of, and the order of constituents in a biopolymer.
National Institutes of Health
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Clinical Data Interchange Standards Consortium Terminology
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2020
Highly Cited
2020
A Novel Coronavirus from Patients with Pneumonia in China, 2019
N. Zhu
,
Dingyu Zhang
,
+15 authors
W. Tan
New England Journal of Medicine
2020
Corpus ID: 210889724
Summary In December 2019, a cluster of patients with pneumonia of unknown cause was linked to a seafood wholesale market in Wuhan…
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Review
2015
Review
2015
limma powers differential expression analyses for RNA-sequencing and microarray studies
Matthew E. Ritchie
,
B. Phipson
,
+4 authors
G. Smyth
Nucleic Acids Research
2015
Corpus ID: 301840
limma is an R/Bioconductor software package that provides an integrated solution for analysing data from gene expression…
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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
2014
Highly Cited
2014
HTSeq—a Python framework to work with high-throughput sequencing data
S. Anders
,
Paul Theodor Pyl
,
W. Huber
bioRxiv
2014
Corpus ID: 6144649
Motivation: A large choice of tools exists for many standard tasks in the analysis of high-throughput sequencing (HTS) data…
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Highly Cited
2013
Highly Cited
2013
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
Yang Liao
,
G. Smyth
,
Wei Shi
Bioinform.
2013
Corpus ID: 15960459
MOTIVATION Next-generation sequencing technologies generate millions of short sequence reads, which are usually aligned to a…
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Highly Cited
2012
Highly Cited
2012
Fast gapped-read alignment with Bowtie 2
Ben Langmead
,
S. Salzberg
Nature Methods
2012
Corpus ID: 205420407
As the rate of sequencing increases, greater throughput is demanded from read aligners. The full-text minute index is often used…
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Highly Cited
2012
Highly Cited
2012
SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing
A. Bankevich
,
S. Nurk
,
+13 authors
P. Pevzner
J. Comput. Biol.
2012
Corpus ID: 12179679
The lion's share of bacteria in various environments cannot be cloned in the laboratory and thus cannot be sequenced using…
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Highly Cited
2009
Highly Cited
2009
The Sequence Alignment/Map format and SAMtools
Heng Li
,
R. Handsaker
,
+6 authors
R. Durbin
Bioinform.
2009
Corpus ID: 2107238
Summary: The Sequence Alignment/Map (SAM) format is a generic alignment format for storing read alignments against reference…
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Highly Cited
2000
Highly Cited
2000
Primer3 on the WWW for general users and for biologist programmers.
S. Rozen
,
H. Skaletsky
Methods in molecular biology
2000
Corpus ID: 39882212
1. Introduction Designing PCR and sequencing primers are essential activities for molecular biologists around the world. This…
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Highly Cited
1998
Highly Cited
1998
Cluster analysis and display of genome-wide expression patterns.
M. Eisen
,
P. Spellman
,
P. Brown
,
D. Botstein
Proceedings of the National Academy of Sciences…
1998
Corpus ID: 3010146
A system of cluster analysis for genome-wide expression data from DNA microarray hybridization is described that uses standard…
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