GRCh38 gene

Aliases

refdata-cellranger-GRCh38-2020-A

External links

NCBI Gene · Ensembl · GeneCards · UniProt

No related entities found.

Mentioned in (18)

Papers in which this entity is mentioned.

• Nanopore-based cell-free DNA fragmentation and methylation profiles from the cerebral spinal fluid of patients with lung cancer brain metastases. (2025)
• Single cell and spatial alternative splicing analysis with Nanopore long read sequencing. (2025)
• Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
• Detecting transposable elements in long-read genomes using sTELLeR. (2024)
• Integrated Single-Cell Multiomic Profiling of Caudate Nucleus Suggests Key Mechanisms in Alcohol Use Disorder. (2024)
• The Application of Long-Read Sequencing to Cancer. (2024)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• The complete sequence of a human genome. (2022)
• Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
• Single-cell genomic variation induced by mutational processes in cancer. (2022)
• Integrative reconstruction of cancer genome karyotypes using InfoGenomeR. (2021)
• Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes. (2020)
• Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
• htsget: a protocol for securely streaming genomic data. (2019)
• A multi-task convolutional deep neural network for variant calling in single molecule sequencing. (2019)
• Best practices for bioinformatic characterization of neoantigens for clinical utility. (2019)
• Nanopore sequencing and assembly of a human genome with ultra-long reads. (2018)
• Extending reference assembly models. (2015)

Merged raw entities (3)

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