Corpus 1,273 assessed · 1,174 scored · 643 reproduced ≥75 · 169 flagged ·∅ 74.1/100

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499 matching publication(s)
Accurate sequence variant genotyping in cattle using variation-aware genome graphs.
PMID 31092189 · Genet Sel Evol · 2019
L1 45/100
Reusable building blocks in biological systems.
PMID 30958230 · J R Soc Interface · 2018
L1 82/100
Sequencing of human genomes with nanopore technology.
PMID 31015479 · Nat Commun · 2019
L1 75/100
Predicting enhancers in mammalian genomes using supervised hidden Markov models.
PMID 30917778 · BMC Bioinformatics · 2019
L1 70/100
SMAGEXP: a galaxy tool suite for transcriptomics data meta-analysis.
PMID 30698691 · Gigascience · 2019
L1 82/100
Nimbus: a design-driven analyses suite for amplicon-based NGS data.
PMID 29538618 · Bioinformatics · 2018
L1 64/100
Bayesian prediction of RNA translation from ribosome profiling.
PMID 28126919 · Nucleic Acids Res · 2017
62/100
Representing and querying disease networks using graph databases.
PMID 27462371 · BioData Min · 2016
L1 77/100
Cell Specific eQTL Analysis without Sorting Cells.
PMID 25955312 · PLoS Genet · 2015
L1 90/100
Conservation and losses of non-coding RNAs in avian genomes.
PMID 25822729 · PLoS One · 2015
L1 100/100
A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm.
PMID 24193348 · European Journal of Human Genetics · 2014
L1 83/100
nf-core/mag: a best-practice pipeline for metagenome hybrid assembly and binning.
PMID 35118380 · NAR Genom Bioinform · 2022
L1 100/100