Demo Data from VLDB 2026 / reviewers in the wild / expert
Markus Hsi-Yang Fritz
dblp:244/8772
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2019
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 1 heaviest of 1, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › sequence analysis
sequencing data analysis |
0.4 | 1 | 2019 | Alfred: interactive multi-sample BAM alignment statistics, feature counting and feature annotation for long- and short-read sequencing · Bioinform. 2019 |
Methods — techniques the papers use, named apart from their topics
read-group aware analysis · 0.4haplotype phasing · 0.4
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2019 | Alfred: interactive multi-sample BAM alignment statistics, feature counting and feature annotation for long- and short-read sequencingabstractSUMMARY: Harmonizing quality control (QC) of large-scale second and third-generation sequencing datasets is key for enabling downstream computational and biological analyses. We present Alfred, an efficient and versatile command-line application that computes multi-sample QC metrics in a read-group aware manner, across a wide variety of sequencing assays and technologies. In addition to standard QC metrics such as GC bias, base composition, insert size and sequencing coverage distributions it supports haplotype-aware and allele-specific feature counting and feature annotation. The versatility of Alfred allows for easy pipeline integration in high-throughput settings, including DNA sequencing facilities and large-scale research initiatives, enabling continuous monitoring of sequence data quality and characteristics across samples. Alfred supports haplo-tagging of BAM/CRAM files to conduct haplotype-resolved analyses in conjunction with a variety of next-generation sequencing based assays. Alfred's companion web application enables interactive exploration of results and comparison to public datasets. AVAILABILITY AND IMPLEMENTATION: Alfred is open-source and freely available at https://tobiasrausch.com/alfred/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Tobias Rausch, Markus Hsi-Yang Fritz, Jan O. Korbel, Vladimir Benes |
Bioinform. | 2 |