Evidence map›Paper›PMID 27153676›Full record

ArticleBioinformatics (Oxford, England)2016

Isoform-level ribosome occupancy estimation guided by transcript abundance with Ribomap.

Hao Wang, Joel McManus, Carl Kingsford

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Hao WangComputational Biology Department, School of Computer Science and.
Joel McManusComputational Biology Department, School of Computer Science and Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, USA.
Carl KingsfordComputational Biology Department, School of Computer Science and.

Funding

Algorithms for Managing Uncertainty in Chromosome Conformation Capture DataR01HG007104 · NHGRI · CARNEGIE-MELLON UNIVERSITY · PI KINGSFORD, CARLETON LEE · 2013 to 2015
$1.3M
Fast k-mer Counting to Quantify Gene Expression and Improve Genome AssemblyR21HG006913 · NHGRI · CARNEGIE-MELLON UNIVERSITY · PI KINGSFORD, CARLETON LEE · 2012 to 2014
$430k
NHGRI NIH HHS R01 HG007104NHGRI NIH HHS R21 HG006913
6 · The paper itself

Abstract

unlabelled: Ribosome profiling is a recently developed high-throughput sequencing technique that captures approximately 30 bp long ribosome-protected mRNA fragments during translation. Because of alternative splicing and repetitive sequences, a ribosome-protected read may map to many places in the transcriptome, leading to discarded or arbitrary mappings when standard approaches are used. We present a technique and software that addresses this problem by assigning reads to potential origins proportional to estimated transcript abundance. This yields a more accurate estimate of ribosome profiles compared with a naïve mapping. AVAILABILITY AND IMPLEMENTATION: Ribomap is available as open source at http://www.cs.cmu.edu/∼ckingsf/software/ribomap CONTACT: carlk@cs.cmu.edu SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

RibosomesAlternative SplicingHigh-Throughput Nucleotide SequencingProtein IsoformsSequence Analysis, RNASoftwareProtein Isoforms

Identifiers

PMID27153676
PMCPMC4908323

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.