Homo sapiens genome reference file based on GRCh37
The Broad Institute created a human genome reference file based on GRCh37. This reference is often referred to as b37 (Homo_sapiens_assembly19.fasta, MD5sum: 886ba1559393f75872c1cf459eb57f2d). When people at The Broad Institute's Genomics Platform refer to the hg19 reference, they are actually referring to b37. This reference contains some alterations from the baseline reference from the Genome Reference Consortium. These alterations largely consist of contig name changes, however there are known sequence differences on some contigs as well.
- 10/05/2023
- 1 sample
- DAC: EGAC50000000003
- Technology: HiSeq X Five
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| Whole Genome Sequencing |
This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.
| ID | File Type | Size | Located in | |
|---|---|---|---|---|
| EGAF50000103833 | fasta | 3.1 GB | ||
| 1 File (3.1 GB) | ||||