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Philipp Rescheneder
Philipp Rescheneder
Center for Integrative Bioinformatics Vienna, University of Vienna, Medical University of Vienna
Verified email at univie.ac.at - Homepage
Title
Cited by
Cited by
Year
Accurate detection of complex structural variations using single-molecule sequencing
FJ Sedlazeck, P Rescheneder, M Smolka, H Fang, M Nattestad, ...
Nature methods 15 (6), 461-468, 2018
12432018
Thiol-linked alkylation of RNA to assess expression dynamics
VA Herzog, B Reichholf, T Neumann, P Rescheneder, P Bhat, TR Burkard, ...
Nature methods 14 (12), 1198-1204, 2017
4552017
NextGenMap: fast and accurate read mapping in highly polymorphic genomes
FJ Sedlazeck, P Rescheneder, A Von Haeseler
Bioinformatics 29 (21), 2790-2791, 2013
3972013
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis
M Muhar, A Ebert, T Neumann, C Umkehrer, J Jude, C Wieshofer, ...
Science 360 (6390), 800-805, 2018
2992018
A-type lamins bind both hetero-and euchromatin, the latter being regulated by lamina-associated polypeptide 2 alpha
K Gesson, P Rescheneder, MP Skoruppa, A von Haeseler, T Dechat, ...
Genome research 26 (4), 462-473, 2016
1862016
Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line
M Nattestad, S Goodwin, K Ng, T Baslan, FJ Sedlazeck, P Rescheneder, ...
Genome research 28 (8), 1126-1135, 2018
1602018
The Borrelia burgdorferi RelA/SpoT Homolog and Stringent Response Regulate Survival in the Tick Vector and Global Gene Expression during Starvation
D Drecktrah, M Lybecker, N Popitsch, P Rescheneder, LS Hall, ...
PLoS Pathogens 11 (9), e1005160, 2015
932015
Quantification of experimentally induced nucleotide conversions in high-throughput sequencing datasets
T Neumann, VA Herzog, M Muhar, A von Haeseler, J Zuber, SL Ameres, ...
BMC bioinformatics 20, 1-16, 2019
862019
Revisiting the coding potential of the E. coli genome through Hfq co-immunoprecipitation
I Bilusic, N Popitsch, P Rescheneder, R Schroeder, M Lybecker
RNA biology 11 (5), 641-654, 2014
842014
Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
N Popitsch, I Bilusic, P Rescheneder, R Schroeder, M Lybecker
BMC genomics 18, 1-14, 2017
492017
Natural RNA polymerase aptamers regulate transcription in E. coli
N Sedlyarova, P Rescheneder, A Magan, N Popitsch, N Rziha, I Bilusic, ...
Molecular cell 67 (1), 30-43. e6, 2017
472017
Teaser: Individualized benchmarking and optimization of read mapping results for NGS data
M Smolka, P Rescheneder, MC Schatz, A von Haeseler, FJ Sedlazeck
Genome biology 16, 1-10, 2015
332015
The Stringent Response-Regulated sRNA Transcriptome of Borrelia burgdorferi
D Drecktrah, LS Hall, P Rescheneder, M Lybecker, DS Samuels
Frontiers in cellular and infection microbiology 8, 231, 2018
242018
Thiol-linked alkylation for the metabolic sequencing of RNA
VA Herzog, B Reichholf, T Neumann, P Rescheneder, P Bhat, TR Burkard, ...
bioRxiv, 177642, 2017
42017
MASon: Million Alignments in Seconds-A Platform Independent Pairwise Sequence Alignment Library for next Generation Sequencing Data
P Rescheneder, A von Haeseler, FJ Sedlazeck
International Conference on Bioinformatics Models, Methods and Algorithms 2 …, 2012
42012
Haplotype-resolved analysis of cancer genomes and epigenomes using Oxford Nanopore sequencing
P Rescheneder, P James, S McKenzie, A Talenti, S Aganezov, D Turner, ...
Cancer Research 84 (6_Supplement), 6218-6218, 2024
2024
Abstract LB081: Concurrent characterization of somatic nucleotide mutations, 5mC, and 5hmC methylation in clinical research samples using a single nanopore sequencing assay
S Aganezov, P Rescheneder, J Beaulaurier, P James, S Juul
Cancer Research 83 (8_Supplement), LB081-LB081, 2023
2023
SV detection, SNP phasing and haplotype methylation calling from one nanopore sequencing dataset provides insights to complex genomic disorder
HM Jeffery, P Rescheneder, D Turner, P James, S Juul
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 554-554, 2022
2022
Directly detect and phase genomic 5mC methylation with high reproducibility and low bias using Nanopore sequencing
R Esteban, IA Vasilescu, MH Stoiber, DJ Turner, D Stoddart, E Harrington, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 549-549, 2022
2022
Performance benchmarking for calling and phasing of single-nucleotide polymorphisms and structural variants using Nanopore sequencing
R Esteban, A Doran, IA Vasilescu, DJ Turner, D Stoddart, S Juul, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 441-442, 2022
2022
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