Evidence map›Paper›PMID 34235432›Full record

ArticleNAR genomics and bioinformatics2021

PIP-SNP: a pipeline for processing SNP data featured as linkage disequilibrium bin mapping, genotype imputing and marker synthesizing.

Wenchao Zhang, Yun Kang, Xinbin Dai, Shizhong Xu, Patrick X Zhao

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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.

Wenchao ZhangNoble Research Institute LLC, 2510 Sam Noble Parkway, Ardmore, OK 73401, USA.
Yun KangNoble Research Institute LLC, 2510 Sam Noble Parkway, Ardmore, OK 73401, USA.
Xinbin DaiNoble Research Institute LLC, 2510 Sam Noble Parkway, Ardmore, OK 73401, USA.
Shizhong XuDepartment of Botany and Plant Sciences, University of California, Riverside, CA 92521, USA.
Patrick X ZhaoNoble Research Institute LLC, 2510 Sam Noble Parkway, Ardmore, OK 73401, USA.ORCID https://orcid.org/0000-0002-3460-5564

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide association study data analyses often face two significant challenges: (i) high dimensionality of single-nucleotide polymorphism (SNP) genotypes and (ii) imputation of missing values. SNPs are not independent due to physical linkage and natural selection. The correlation of nearby SNPs is known as linkage disequilibrium (LD), which can be used for LD conceptual SNP bin mapping, missing genotype inferencing and SNP dimension reduction. We used a stochastic process to describe the SNP signals and proposed two types of autocorrelations to measure nearby SNPs' information redundancy. Based on the calculated autocorrelation coefficients, we constructed LD bins. We adopted a

Identifiers

PMID34235432
PMCPMC8256826

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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.