Evidence map›Paper›PMID 31834373›Full record

ArticleBioinformatics (Oxford, England)2020

HaploTypo: a variant-calling pipeline for phased genomes.

Cinta Pegueroles, Verónica Mixão, Laia Carreté, Manu Molina, Toni Gabaldón

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Journal of fungi (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Article
  7. Genome analysis of Candida subhashii reveals its hybrid nature and dual mitochondrial genome conformations.DNA research : an international journal for rapid publication of reports on genes and genomes · 2021
    Article
  8. Article
  9. Article
  10. Article
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

5 authors.

Cinta PeguerolesCentre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona 08003, Spain.
Verónica MixãoCentre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona 08003, Spain.
Laia CarretéCentre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona 08003, Spain.
Manu MolinaCentre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona 08003, Spain.
Toni GabaldónCentre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona 08003, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summaryAn increasing number of phased (i.e. with resolved haplotypes) reference genomes are available. However, the most genetic variant calling tools do not explicitly account for haplotype structure. Here, we present HaploTypo, a pipeline tailored to resolve haplotypes in genetic variation analyses. HaploTypo infers the haplotype correspondence for each heterozygous variant called on a phased reference genome. AVAILABILITY AND IMPLEMENTATION: HaploTypo is implemented in Python 2.7 and Python 3.5, and is freely available at https://github.com/gabaldonlab/haplotypo, and as a Docker image. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

GenomeSoftwareHaplotypesHeterozygote

Identifiers

PMID31834373
PMCPMC7178392

What OpenQuestion holds

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LicenceCC BY-NC
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.