diff --git a/content/3.genomics-platform/2.about-our-data/1.data-sets-and-data-access-units.md b/content/3.genomics-platform/2.about-our-data/1.data-sets-and-data-access-units.md index f42a501..21713fa 100644 --- a/content/3.genomics-platform/2.about-our-data/1.data-sets-and-data-access-units.md +++ b/content/3.genomics-platform/2.about-our-data/1.data-sets-and-data-access-units.md @@ -126,6 +126,7 @@ The following data set(s) are included within PCGP: - [Clinical Pilot](#clinical-pilot) - [DMG-H3K27a Clonal Evolution (H3K27A_EVOLUTION)](#dmg-h3k27a-clonal-evolution) - [Genome 4 Kids (G4K)](#genome-4-kids) +- [G4KF](#g4kffpe) - [Genomics and Transcriptomics of Relapsed Pediatric AML (RPAML)](#genomics-and-transcriptomics-of-relapsed-pediatric-aml-rpaml) - [Landscape of Pediatric Acute Myeloid Leukemia (PanpAML)](#landscape-of-pediatric-acute-myeloid-leukemia-panpaml) - [Medulloblastoma Preclinical Ribociclib and Gemcitabine (MBPRG)](#medulloblastoma-preclinical-ribociclib-and-gemcitabine-mbprg) @@ -168,7 +169,8 @@ Additional information can also be seen including which [Data Access Units (DAU) | [Clinical Pilot](#clinical-pilot) | PCGP, Clinical Genomics | Paired Tumor-Normal | WGS, WES, RNA-Seq | 155 | | [CReATe](#clinical-research-in-als-and-related-disorders-for-therapeutic-development-consortium) | CReATe | PBMC Germline DNA | WGS | 705 | | [CSTN](#childhood-solid-tumor-network) | PCGP, Clinical Genomics | Paired Tumor-Normal | WGS, WES, RNA-Seq | 143 | -| [G4K](#genome-4-kids) | PCGP, Clinical Genomics | Paired Tumor-Normal | WGS, WES, RNA-Seq | 571 | +| [G4K](#genome-4-kids) | PCGP, Clinical Genomics | Paired Tumor-Normal | WGS, WES, RNA-Seq | 565 | +| [G4KF](#g4kffpe) | PCGP | — | WES | 33 | | [H3K27A_EVOLUTION](#dmg-h3k27a-clonal-evolution) | PCGP | — | WGS, WES | 70 | | [MBPRG](#medulloblastoma-preclinical-ribociclib-and-gemcitabine-mbprg) | PCGP | — | RNA-Seq | 70 | | [MBPRP](#medulloblastoma-preclinical-ribociclib-and-paxalisib-mbprp) | PCGP | — | RNA-Seq | 39 | @@ -178,7 +180,7 @@ Additional information can also be seen including which [Data Access Units (DAU) | [PCGP](#pediatric-cancer-genome-project) | PCGP | Paired Tumor-Normal | WGS, WES, RNA-Seq | 3,031 | | [PedAML](#pediatric-acute-myeloid-leukemia-pedaml) | PCGP | — | WES, WGS, RNA-Seq | 275 | | [RPAML](#genomics-and-transcriptomics-of-relapsed-pediatric-aml-rpaml) | PCGP, Clinical Genomics | — | WGS, RNA-Seq | 265 | -| [RTCG](#real-time-clinical-genomics) | PCGP, Clinical Genomics | Paired Tumor-Normal | WGS, WES, RNA-Seq | 2,371 | +| [RTCG](#real-time-clinical-genomics) | PCGP, Clinical Genomics | Paired Tumor-Normal | WGS, WES, RNA-Seq | 7,767 | | [SGP](#sickle-cell-genome-project) | SGP | Germline Only | WGS | 807 | | [SJLIFE](#st-jude-life) | SJLIFE | Germline Only | WGS, WES | 4,838 | | [SJLIFE_ClonalHematopoiesis](#st-jude-life-clonal-hematopoiesis) | SJLIFE | — | Single Cell-WGS, Targeted | 3,192 | @@ -268,6 +270,10 @@ For more information see: [http://permalinks.stjude.cloud/permalinks/h3k27a_evol The goal of the Genomes 4 Kids (G4K) prospective study was to determine whether the three-platform sequencing protocol laid out in the Clinical Pilot project could generate results on a clinical timeline in practice and to evaluate the prevalence of actionable findings. The study concluded with just over 300 patients, and the publication is currently in review. +### G4KFFPE + +**DAU**: PCGP | **Tissue Type**: — | **Sequencing Type**: WES | **Samples**: 33 + ### Genomics and Transcriptomics of Relapsed Pediatric AML (RPAML) **DAU**: Clinical Genomics, PCGP | **Tissue Type**: — | **Sequencing Type**: RNA-seq, WGS | **Samples**: 265 diff --git a/content/3.genomics-platform/2.about-our-data/3.metadata-and-clinical-information.md b/content/3.genomics-platform/2.about-our-data/3.metadata-and-clinical-information.md index b701467..522909a 100644 --- a/content/3.genomics-platform/2.about-our-data/3.metadata-and-clinical-information.md +++ b/content/3.genomics-platform/2.about-our-data/3.metadata-and-clinical-information.md @@ -18,7 +18,7 @@ Properties with `attr` prepended are information queried from the physician or r | `file_id` | A unique identifier for the file on DNAnexus, you can see this value listed as “ID” in the DNAnexus user interface. | | `subject_name` | A unique subject identifier assigned internally at St. Jude. | | `sample_name` | A unique sample identifier assigned internally at St. Jude. | -| `sample_type` | One of Autopsy, Cell line, Diagnosis, Germline, Metastasis, Relapse, or Xenograft. | +| `sample_type` | One of Autopsy, Cell line, Diagnosis, Germline, Metastasis, Post-Transplant, Relapse, Xenograft or Other. | | `sequencing_type` | Whether the file was generated from Whole Genome (WGS), Whole Exome (WES), or RNA-Seq. | | `file_type` | Specifies the type of file. Note that index files will be labeled as the file type they accompany and will automatically be selected together in our data browser. If you wish to distinguish between the two in your project, please parse the `file_path` where index files are appended with an additional string, such as `.bai`. | | `description` | Optional field that may contain additional file information. |