Manuel Holtgrewe

Orcid: 0000-0002-3051-1763

According to our database1, Manuel Holtgrewe authored at least 16 papers between 2010 and 2022.

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Bibliography

2022
ClearCNV: CNV calling from NGS panel data in the presence of ambiguity and noise.
Bioinform., 2022

2021
Sustainable data analysis with Snakemake.
F1000Research, 2021

2020
VarFish: comprehensive DNA variant analysis for diagnostics and research.
Nucleic Acids Res., 2020

SODAR Core: a Django-based framework for scientific data management and analysis web apps.
J. Open Source Softw., 2020

DigestiFlow: from BCL to FASTQ with ease.
Bioinform., 2020

2019
AltamISA: a Python API for ISA-Tab files.
J. Open Source Softw., 2019

2017
HLA-MA: simple yet powerful matching of samples using HLA typing results.
Bioinform., 2017

2016
VCFPy: a Python 3 library with good support for both reading and writing VCF.
J. Open Source Softw., 2016

2015
Engineering Algorithms for Personal Genome Pipelines.
PhD thesis, 2015

Methods for the detection and assembly of novel sequence in high-throughput sequencing data.
Bioinform., 2015

2014
Genome alignment with graph data structures: a comparison.
BMC Bioinform., 2014

Fiona: a parallel and automatic strategy for read error correction.
Bioinform., 2014

2012
RazerS 3: Faster, fully sensitive read mapping.
Bioinform., 2012

2011
A Novel And Well-Defined Benchmarking Method For Second Generation Read Mapping.
BMC Bioinform., 2011

2010
Engineering a scalable high quality graph partitioner.
Proceedings of the 24th IEEE International Symposium on Parallel and Distributed Processing, 2010

Simple and Fast Nearest Neighbor Search.
Proceedings of the Twelfth Workshop on Algorithm Engineering and Experiments, 2010


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