Cited by 993Genomics and Phylogenetic StudiesGenomics and Rare DiseasesGenetics, Bioinformatics, and Biomedical Research

Next-generation DNA sequencing techniques

Open access
Ansorge, Wilhelm J.·2009·New Biotechnology

Abstract

Next-generation high-throughput DNA sequencing techniques are opening fascinating opportunities in the life sciences. Novel fields and applications in biology and medicine are becoming a reality, beyond the genomic sequencing which was original development goal and application. Serving as examples are: personal genomics with detailed analysis of individual genome stretches; precise analysis of RNA transcripts for gene expression, surpassing and replacing in several respects analysis by various microarray platforms, for instance in reliable and precise quantification of transcripts and as a tool for identification and analysis of DNA regions interacting with regulatory proteins in functional regulation of gene expression. The next-generation sequencing technologies offer novel and rapid ways for genome-wide characterisation and profiling of mRNAs, small RNAs, transcription factor regions, structure of chromatin and DNA methylation patterns, microbiology and metagenomics. In this article, development of commercial sequencing devices is reviewed and some European contributions to the field are mentioned. Presently commercially available very high-throughput DNA sequencing platforms, as well as techniques under development, are described and their applications in bio-medical fields discussed.

Integrity signals

Registry

Crossref · 10.1016/j.nbt.2008.12.009

Cites

26 of 26 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Particularly in the last 25 years, there has been an ever increasing number of ALE experiments with Escherichia coli and Saccharomyces cerevisiae being the most prominent organisms under investigation.

    “however, particularly in the last 25 years, there has been an ever increasing number of such experiments with Escherichia coli and Saccharomyces cerevisiae being the most prominent organisms under investigation [26-28].”

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Ansorge, W. J.
Affiliations
École Polytechnique Fédérale de Lausanne (CH)
Corresponding author
Ansorge, Wilhelm J.
Venue
New Biotechnology
Publisher
Elsevier BV
Published
2009-04
Volume
25
Issue
4
Pages
195-203
ISSN
1871-6784 (ISSN-L)
OpenAlex
W2058839892
Cited by
993
References
26
Citations by year
2026: 3 · 2025: 27 · 2024: 22 · 2023: 28 · 2022: 27 · 2021: 55 · 2020: 64 · 2019: 56 · 2018: 59 · 2017: 51 · 2016: 61 · 2015: 80 · 2014: 74 · 2013: 92 · 2012: 78
FWCI
39.25
Type
journal article
Language
en
Open access
Locations
  • New Biotechnology (publishedVersion)
  • PubMed (publishedVersion)
  • Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
  • Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genetics, Bioinformatics, and Biomedical Research
Keywords
next-generation sequencing, sequencing platforms, personal genomics, RNA sequencing, gene expression profiling, transcript quantification, protein-DNA interactions, metagenomics, DNA methylation, chromatin structure, small RNA, transcription factors
MeSH terms
Chromosome Mapping, Sequence Alignment, Sequence Analysis, DNA

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review