Evidence map›Paper›PMID 27855707›Full record

ArticleGenome biology2016

A novel codon-based de Bruijn graph algorithm for gene construction from unassembled transcriptomes.

Gongxin Peng, Peifeng Ji, Fangqing Zhao

Abstract read
In one paragraph

Article in Genome biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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.

Gongxin PengComputational Genomics Lab, Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China.
Peifeng JiComputational Genomics Lab, Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China.
Fangqing ZhaoComputational Genomics Lab, Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China. zhfq@biols.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most gene prediction methods detect coding sequences from transcriptome assemblies in the absence of closely related reference genomes. Such methods are of limited application due to high transcript fragmentation and extensive assembly errors, which may lead to redundant or false coding sequence predictions. We present inGAP-CDG, which can construct full-length and non-redundant coding sequences from unassembled transcriptomes by using a codon-based de Bruijn graph to simplify the assembly process and a machine learning-based approach to filter false positives. Compared with other methods, inGAP-CDG exhibits a significant increase in predicted coding sequence length and robustness to sequencing errors and varied read length.

Indexed as

Computational BiologySequence Analysis, RNASoftwareAlgorithmsCodonHigh-Throughput Nucleotide SequencingOpen Reading FramesPancreatitis-Associated ProteinsTranscriptomeCodonPancreatitis-Associated ProteinsREG3A protein, humande Bruijn graphGene predictionPhylogenomicsTranscriptome

Identifiers

PMID27855707
PMCPMC5114782

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.