Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Cloud computing-based TagSNP selection algorithm for human genome data.

International journal of molecular sciences - 5 Jan 2015

Hung Che-Lun, Chen Wen-Pei, Hua Guan-Jie, Zheng Huiru, Tsai Suh-Jen Jane, Lin Yaw-Ling

Abstract excerpt

Single nucleotide polymorphisms (SNPs) play a fundamental role in human genetic variation and are used in medical diagnostics, phylogeny construction, and drug design. They provide the highest-resolution genetic fingerprint for identifying disease associations and human features. Haplotypes are regions of linked genetic variants that are closely spaced on the genome and tend to be inherited together. Genetics...

Topics

Algorithms
Computational Biology
Genome, Human
Genome-Wide Association Study
Haplotypes
Humans
Linkage Disequilibrium
Polymorphism, Single Nucleotide

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25569088
DOI: 10.3390/ijms16011096
PMCID: PMC4307292

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-25569088-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cloud computing-based TagSNP selection algorithm for human genome data.PMID 25569088Read ↗

Novel and efficient tag SNPs selection algorithms.Semantic proximity Read ↗

Searching for SNPs with cloud computing.Semantic proximity Read ↗

DiGeST: Distributed Computing for Scalable Gene and Variant Ranking with Hadoop/SparkSemantic proximity Read ↗

SeqsLab: an integrated platform for cohort-based annotation and interpretation of genetic variants on SparkSemantic proximity Read ↗

A Fast and Scalable Workflow for SNPs Detection in Genome Sequences Using Hadoop Map-Reduce.Semantic proximity Read ↗

Inexpensive and Highly Reproducible Cloud-Based Variant Calling of 2,535 Human Genomes.Semantic proximity Read ↗

Cloud‐Based GWAS Platform: An Innovative Solution for Efficient Acquisition and Analysis of Genomic DataSemantic proximity Read ↗

BlueSNP: R package for highly scalable genome-wide association studies using Hadoop clusters.Semantic proximity Read ↗

A novel approach for the identification of single nucleotide polymorphisms.Semantic proximity Read ↗

High-performance web services for querying gene and variant annotation.Semantic proximity Read ↗

eCEO: an efficient Cloud Epistasis cOmputing model in genome-wide association study.Semantic proximity Read ↗

Benchmarking undedicated cloud computing providers for analysis of genomic datasetsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.