D. Parkhomchuk

发表

Transcriptome analysis by strand-specific sequencing of complementary DNA

T. Borodina, H. Lehrach, S. Krobitsch, 2009, Nucleic acids research.

A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome

Marcel H. Schulz, S. Haas, H. Lehrach, 2008, Science.

Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer.

V. Beneš, C. von Kalle, R. Eils, 2013, Cancer cell.

Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis

H. Lehrach, K. Zatloukal, D. Parkhomchuk, 2009, PloS one.

Use of high throughput sequencing to observe genome dynamics at a single cell level

D. Parkhomchuk, V. Amstislavskiy, V. Ogryzko, 2009, Proceedings of the National Academy of Sciences.

A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT.

P. Robinson, S. Mundlos, D. Parkhomchuk, 2013, Blood.

Key Point : A carrier of a deleterious splice site mutation in PIGT acquired a second hit in PIGT and developed PNH

P. Robinson, S. Mundlos, D. Parkhomchuk, 2013 .

PIGT mutation and a somatic mutation in A case of paroxysmal nocturnal hemoglobinuria caused by a germline

P. Robinson, S. Mundlos, D. Parkhomchuk, 2013 .

Positional Information Storage in Sequence Patterns

D. Parkhomchuk, A. Grigoriev, A. Shadrin, 2013 .

Estimating exome genotyping accuracy by comparing to data from large scale sequencing projects

Tom Kamphans, Thorsten Dickhaus, Verena Heinrich, 2013, Genome Medicine.

Genetic recombination as DNA repair

D. Parkhomchuk, A. Mchardy, A. Shadrin, 2015, bioRxiv.

Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome

P. Robinson, S. Mundlos, D. Parkhomchuk, 2014, Molecular genetics & genomic medicine.

Drake’s rule as a consequence of approaching channel capacity

D. Parkhomchuk, A. Shadrin, 2013, Naturwissenschaften.

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Andreas Busjahn, Jens Jordan, Herbert Schulz, 2015, Nature Genetics.

Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool.

D. Parkhomchuk, J. Hentschel, H. Peters, 2016, Gene.

Position-Associated GC Asymmetry of Gene Duplicates

D. Parkhomchuk, S. Rodin, 2004, Journal of Molecular Evolution.

Filtering for Compound Heterozygous Sequence Variants in Non-Consanguineous Pedigrees

Tom Kamphans, Na Zhu, Peter M. Krawitz, 2013, PloS one.

Epigenetic Changes and Repositioning Determine the Evolutionary Fate of Duplicated Genes

A. Riggs, D. Parkhomchuk, S. Rodin, 2005, Biochemistry (Moscow).

Repositioning-dependent fate of duplicate genes.

A. Riggs, D. Parkhomchuk, S. Rodin, 2005, DNA and cell biology.

Darwinian Genetic Drift

D. Parkhomchuk, A. Shadrin, 2017, 1701.02988.

Two Major Paths of Gene-Duplicates Evolution

D. Parkhomchuk, S. Rodin, 2004, q-bio/0410025.

Estimating exome genotyping accuracy by comparing to data from large scale sequencing projects

T. Dickhaus, P. Robinson, D. Parkhomchuk, 2013 .

Fast and memory-efficient noisy read overlapping with KD-trees

Alice C. McHardy, Andreas Bremges, Dmitri V. Parkhomchuk, 2017, bioRxiv.