seqr : A web‐based analysis and collaboration tool for rare disease genomics is a research paper published in Human Mutation (2022). On theSindex it has a DataRank of 0. It has been cited 112 times.
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NIH HHS
Grant: U01HG011755
NHGRI NIH HHS
Grant: UM1 HG008900
NHGRI NIH HHS
Grant: R01 HG009141
NHGRI NIH HHS
Grant: U24 HG010262
National Institutes of Health
Grant: 5UM1HG008900-04
Joint Center for Mendelian Genomics
National Institutes of Health
Grant: 5U24HG010262-03
The AnVIL Data Ecosystem
National Institutes of Health
Grant: 5U01HG011755-03
Broad Institute Mendelian Genomic Research Center
National Institutes of Health
Grant: 5R01HG009141-02
A powerful web-based discovery platform for rare disease genetics
FWCI
16.80
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 1 of Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue
Additional file 1 of Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue
Additional file 2 of Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue
Additional file 2 of Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue
Additional file 3 of Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue
Additional file 3 of Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue
Additional file 4 of Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue
Additional file 4 of Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue