Reference health

QUARTIC: QUick pArallel algoRithms for high-Throughput sequencIng data proCessing

https://doi.org/10.12688/f1000research.22954.3
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16/16 checkable references clean · checked 2026-07-14

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a publisher retraction, withdrawal, or removal notice.

3 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 16 checked references that resolve
resolves10.1145/1468075.1468121
Sorting networks and their applications
resolves10.1109/71.642949
Efficient algorithms for all-to-all communications in multiport message-passing systems
resolves10.1093/bioinformatics/btv179
Halvade: scalable sequence analysis with MapReduce
resolves10.1016/0167-8191(96)00024-5
A high-performance, portable implementation of the MPI message passing interface standard
resolves10.1371/journal.pone.0126321
Leveraging the Power of High Performance Computing for Next Generation Sequencing Data Analysis: Tricks and Twists from a High Throughput Exome Workflow
resolves10.4172/0974-8369.1000395
Generations of Sequencing Technologies: From First to Next Generation
resolves10.1109/ICPADS.2001.934815
Communication-efficient bitonic sort on a distributed memory parallel computer
resolves10.1093/bioinformatics/btp698
Fast and accurate long-read alignment with Burrows–Wheeler transform
resolves10.1093/bioinformatics/btp352
The Sequence Alignment/Map format and SAMtools
resolves10.1093/bioinformatics/btp336
SOAP2: an improved ultrafast tool for short read alignment
resolves10.1093/bib/bby051
Review of applications of high-throughput sequencing in personalized medicine: barriers and facilitators of future progress in research and clinical application
resolves10.1101/gr.107524.110
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
resolves10.1093/bioinformatics/btu071
Supercomputing for the parallelization of whole genome analysis
resolves10.1016/j.ajhg.2018.11.014
Integrating Genomics into Healthcare: A Global Responsibility
resolves10.1093/bioinformatics/btv098
Sambamba: fast processing of NGS alignment formats
resolves10.1038/nbt.2835
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
The 3 references without a DOI — listed, not checked
no DOI — not checkedIntroduction to Parallel Computing
no DOI — not checkedbioinfo-pf-curie/mpibwa: version-1.1
no DOI — not checkedbioinfo-pf-curie/mpisort: version-1.4
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a publisher retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

checked 2026-07-14 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record

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