Single Nucleotide Variation Context in Human Genome

EasyChair Preprints
doi 10.29007/mk44
Full Text
Abstract

Available in full text

Date
Authors
Publisher

EasyChair

Related search

Context Complexity of Sites Containing Single Nucleotide Polymorphisms in Human Genome

2019English

EFIN: Predicting the Functional Impact of Nonsynonymous Single Nucleotide Polymorphisms in Human Genome

BMC Genomics
BiotechnologyGenetics
2014English

Accurate Identification of Single-Nucleotide Variants in Whole-Genome-Amplified Single Cells

Nature Methods
BiochemistryBiotechnologyCell BiologyMolecular Biology
2017English

Mitochondria Single Nucleotide Variation Across Six Blood Cell Types

Mitochondrion
Molecular MedicineCell BiologyMolecular Biology
2016English

Genome-Wide Single-Nucleotide Polymorphism Analysis Defines Haplotype Patterns in Mouse

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2003English

Comprehensive Analysis of Single Nucleotide Polymorphisms in Human MicroRNAs

PLoS ONE
Multidisciplinary
2013English

A Framework for Annotating Human Genome in Disease Context

PLoS ONE
Multidisciplinary
2012English

Detection of Large-Scale Variation in the Human Genome

Nature Genetics
Genetics
2004English

VCS: Tool for Visualizing Copy Number Variation and Single Nucleotide Polymorphism

Asian-Australasian Journal of Animal Sciences
Animal ScienceZoologyFood Science
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy