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Fatma Kahveci

Researcher at Bilkent University

Publications -  6
Citations -  17892

Fatma Kahveci is an academic researcher from Bilkent University. The author has contributed to research in topics: Genome-wide association study & Structural variation. The author has an hindex of 3, co-authored 6 publications receiving 12405 citations.

Papers
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Journal ArticleDOI

A global reference for human genetic variation.

Adam Auton, +517 more
- 01 Oct 2015 - 
TL;DR: The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations, and has reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole-generation sequencing, deep exome sequencing, and dense microarray genotyping.

A global reference for human genetic variation

Adam Auton, +479 more
TL;DR: The 1000 Genomes Project as mentioned in this paper provided a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations, and reported the completion of the project, having reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole genome sequencing, deep exome sequencing and dense microarray genotyping.
Journal ArticleDOI

An integrated map of structural variation in 2,504 human genomes

Peter H. Sudmant, +87 more
- 01 Oct 2015 - 
TL;DR: In this paper, the authors describe an integrated set of eight structural variant classes comprising both balanced and unbalanced variants, which are constructed using short-read DNA sequencing data and statistically phased onto haplotype blocks in 26 human populations.
Journal ArticleDOI

Zebrafish brain RNA sequencing reveals that cell adhesion molecules are critical in brain aging

TL;DR: This study investigated the gene expression changes in zebrafish brains through young-adult to adult, and adult to old age, and observed that the expression change of 2 genes, GJC2 and ALCAM, during the aging process was consistent in all experimental sets.
Book ChapterDOI

Whole-Genome Shotgun Sequence CNV Detection Using Read Depth.

TL;DR: A guideline for a user friendly tool for detecting large segmental duplications and deletions that can also predict integer copy numbers for duplicated genes is provided.