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PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

Genome biology(2021)10.1186/s13059-021-02486-wSource: DataRank Database

PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation is a research paper published in Genome biology (2021). On theSindex it has a DataRank of 0.604. It has been cited 55 times.

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0.604DataRank · unranked

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Open Access55 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 3.24)OA: goldTopics (58)Linked Datasets (25)DataCite Reuse (25)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.604

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (4)

HarshaVardhan Doddapaneni ORCID,Winston Timp ORCID,Fritz J. Sedlazeck ORCID,Medhat Mahmoud ORCID

Live enrichment

PubMed:34521442 PMC:PMC8442460 OpenAlex:https://openalex.org/W3199386036

National Institutes of Health

Grant: UM1 HG008898

NHGRI NIH HHS

Grant: R01 HG009190

National Institutes of Health

Grant: 3UM1HG008898-01S3

Genomic Architecture of Common Disease in Diverse Populations

FWCI

3.24

Citation Percentile

0.9%

Citation Trend

2021

2022

2023

2024

2025

2026

goldLicense: cc-by

journalhttps://genomebiology.biomedcentral.com/track/pdf/10.1186/s13059-021-02486-w

GOLDhttps://genomebiology.biomedcentral.com/track/pdf/10.1186/s13059-021-02486-w

publisherhttps://genomebiology.biomedcentral.com/track/pdf/10.1186/s13059-021-02486-w

publisherhttps://link.springer.com/content/pdf/10.1186/s13059-021-02486-w.pdf

publisherhttps://link.springer.com/article/10.1186/s13059-021-02486-w/fulltext.html

Fields of Study

Genomics and Phylogenetic StudiesRNA modifications and cancerGenetic Associations and EpidemiologyMedicineBiologyComputer Science0301 basic medicine03 medical and health sciencesCharcot-Marie-Tooth DiseaseDNA MethylationGenetic VariationGenome, HumanHaplotypesHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNASoftware

MeSH Terms

Charcot-Marie-Tooth DiseaseHaplotypesHumansSoftwareGenetic VariationGenome, HumanSequence Analysis, DNADNA MethylationHigh-Throughput Nucleotide Sequencing

Keywords

BiologyStructural variationComputational biologyHaplotypeMethylationHuman geneticsGeneticsWorkflowSet (abstract data type)Evolutionary biologyGeneComputer scienceGenomeAllelePhasingPacbioSingle-nucleotide VariantOxford NanoporeStructural VariantQH301-705.5Genome, HumanMethodGenetic VariationHigh-Throughput Nucleotide SequencingSequence Analysis, DNAQH426-470DNA MethylationHaplotypesCharcot-Marie-Tooth DiseaseHumansBiology (General)Software

Sustainable Development Goals

SDG 3: 3. Good health

Additional file 1 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16620990.v1figshare

Additional file 1 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16620990figshare

Additional file 21 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16620996.v1figshare

Additional file 21 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16620996figshare

Additional file 1 of FixItFelix: improving genomic analysis by fixing reference errors

10.6084/m9.figshare.22612903figshare

Additional file 1 of FixItFelix: improving genomic analysis by fixing reference errors

10.6084/m9.figshare.22612903.v1figshare

Additional file 3 of FixItFelix: improving genomic analysis by fixing reference errors

10.6084/m9.figshare.22612909.v1figshare

Additional file 3 of FixItFelix: improving genomic analysis by fixing reference errors

10.6084/m9.figshare.22612909figshare

Additional file 1 of Genomic variant benchmark: if you cannot measure it, you cannot improve it

10.6084/m9.figshare.24257470.v1figshare

Additional file 1 of Genomic variant benchmark: if you cannot measure it, you cannot improve it

10.6084/m9.figshare.24257470figshare

Additional file 7 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621014.v1figshare

Additional file 8 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621017.v1figshare

Additional file 9 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621020.v1figshare

Additional file 9 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621020figshare

Additional file 7 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621014figshare

Additional file 8 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621017figshare

Additional file 6 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621011.v1figshare

Additional file 5 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621008.v1figshare

Additional file 5 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621008figshare

Additional file 6 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

10.6084/m9.figshare.16621011figshare

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PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

FAIR Checklist

DataRank Breakdown

Authors (4)

Funding (3 grants)

Impact

Open Access

Topics

Linked Datasets (25)

Annotations (Europe PMC)

Related Papers (7)