On the public citation graph

Hardy Weinberg Exact Test In Large Scale Variant Calling Quality Control

https://doi.org/10.1101/095521
0 signed · 27 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471250953.bi1110s43openalex-snapshot
From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline
inferredcites →https://doi.org/10.1007/bf02981502openalex-snapshot
An exact test for randomness of mating
inferredcites →https://doi.org/10.1016/j.ajhg.2013.11.005openalex-snapshot
Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes
inferredcites →https://doi.org/10.1016/j.cell.2011.09.008openalex-snapshot
Clan Genomics and the Complex Architecture of Human Disease
inferredcites →https://doi.org/10.1038/nature09534openalex-snapshot
A map of human genome variation from population-scale sequencing
inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot
A global reference for human genetic variation
inferredcites →https://doi.org/10.1038/nature19057openalex-snapshot
Analysis of protein-coding genetic variation in 60,706 humans
inferredcites →https://doi.org/10.1038/nrg2986openalex-snapshot
Genotype and SNP calling from next-generation sequencing data
inferredcites →https://doi.org/10.1086/429864openalex-snapshot
A Note on Exact Tests of Hardy-Weinberg Equilibrium
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp698openalex-snapshot
Fast and accurate long-read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1101/gr.146084.112openalex-snapshot
An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data
inferredcites →https://doi.org/10.1101/gr.157388.113openalex-snapshot
Estimating inbreeding coefficients from NGS data: Impact on genotype calling and allele frequency estimation
inferredcites →https://doi.org/10.1101/gr.176552.114openalex-snapshot
An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data
inferredcites →https://doi.org/10.1111/j.1469-1809.2006.00267.xopenalex-snapshot
The Merits of Testing Hardy‐Weinberg Equilibrium in the Analysis of Unmatched Case‐Control Data: A Cautionary Note
inferredcites →https://doi.org/10.1161/circgenetics.108.829747openalex-snapshot
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
inferredcites →https://doi.org/10.1186/1471-2105-12-1openalex-snapshot
MTML-msBayes: Approximate Bayesian comparative phylogeographic inference from multiple taxa and multiple loci with rate heterogeneity
inferredcites →https://doi.org/10.1186/1471-2105-12-231openalex-snapshot
Estimation of allele frequency and association mapping using next-generation sequencing data
inferredcites →https://doi.org/10.1186/1471-2105-15-1openalex-snapshot
New mini- zincin structures provide a minimal scaffold for members of this metallopeptidase superfamily
inferredcites →https://doi.org/10.1186/1471-2105-15-30openalex-snapshot
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
inferredcites →https://doi.org/10.1186/s12859-015-0844-1openalex-snapshot
Weakly supervised learning of biomedical information extraction from curated data
inferredcites →https://doi.org/10.1186/s12859-016-1211-6openalex-snapshot
A hybrid computational strategy to address WGS variant analysis in >5000 samples
inferredcites →https://doi.org/10.1214/aoms/1177730093openalex-snapshot
On a Matching Problem Arising in Genetics
inferredcites →https://doi.org/10.1515/sagmb-2012-0039openalex-snapshot
The mid p-value in exact tests for Hardy-Weinberg equilibrium
inferredcites →https://doi.org/10.1534/genetics.108.088005openalex-snapshot
Distributions of Hardy–Weinberg Equilibrium Test Statistics

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1038/s41598-019-52614-7openalex-snapshot
Empirical design of a variant quality control pipeline for whole genome sequencing data using replicate discordance
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.