Table of Contents
With the support of the Neurofibromatosis Therapeutic Acceleration Program (NTAP), we are excited to introduce a pilot initiative aimed at uniformly processing of genomic and transcriptomic data on the NF Data Portal. This initiative encompasses all projects that have received funding from NTAP between 2018 and 2023. The processing of high-dimensional genomic and transcriptomic data will be carried out through the use of standardized data processing pipelines. By ensuring uniformity in data processing, we will be able to share the processed data on the NF Data Portal and facilitate its utilization in other data analysis and exploration platforms. If you have a dataset shared on the NF Data Portal and would like to utilize the NF-OSI Processing pipelines, please reach out to us at nf-osi@sagebionetworks.org. We would be happy to assist you in a case-by-case basis.
Datatypes eligible for processing
Whole Exome Sequencing
Whole Genome Sequencing
Bulk RNA Sequencing
Single cell RNA sequencing
Required annotations for data files to be staged for processing
For each of the following assays, data files must be annotated with the terms listed below.
RNA Sequencing
Annotation term | Additional Details | |
---|---|---|
1 | fileFormat | Accepted file formats include "fastq", "bam", and "cram". If provided raw data are “bam” or “cram” format, only files that have not undergone any additional filtering (i.e. retains unmapped reads, have not been trimmed, etc) will be eligible for processing. |
2 | individualID | Individual IDs are necessary to create the sample sheets. |
3 | specimenID | specimen IDs are necessary to interpret the analysis. |
4 | Assay | Choose between Bulk RNA Seq or Single Cell RNA Seq. |
5 | Species | The corresponding genome requires knowledge of the species. |
6 | libraryPreparationMethod | This refers to the name of the library preparation, such as KAPA Hyper PCR 3. |
7 | Platform | This refers to the name of the platform used, for example, illumina. |
8 | readPair | Specify whether the read pair is 1 or 2. |
9 | specimenPreparationMethod | Minimize RNA degradation with methods such as flash freezing or RNALater. FFPE is not recommended. |
10 | tumorType | If the tissue is normal, indicate "not applicable." Otherwise, specify the tumor type. |
11 | isStranded* | This answer should be either "yes" or "no." |
12 | readPairOrientation* | Indicate the read pair orientation, such as forward or reverse. |
* optional but recommended
Whole Genome Sequencing
Annotation term | Additional Details | |
---|---|---|
1 | fileFormat | Accepted file formats include "fastq", "bam", and "cram". If provided raw data are “bam” or “cram” format, only files that have not undergone any additional filtering (i.e. retains unmapped reads, have not been trimmed, etc) will be eligible for processing. |
2 | individualID | Individual IDs are necessary to create the sample sheets. |
3 | specimenID | specimen IDs are necessary to interpret the analysis. |
4 | Assay | Choose between Bulk RNA Seq or Single Cell RNA Seq. |
5 | Species | The corresponding genome requires knowledge of the species. |
6 | libraryPreparationMethod | This refers to the name of the library preparation, such as KAPA Hyper PCR 3. |
7 | Platform | This refers to the name of the platform used, for example, illumina. |
8 | readPair | Specify whether the read pair is 1 or 2. |
9 | specimenPreparationMethod | Minimize RNA degradation with methods such as flash freezing or RNALater. FFPE is not recommended. |
10 | tumorType | If the tissue is normal, indicate "not applicable." Otherwise, specify the tumor type. NOTE: Files from samples lacking tumor-normal pairs will not be eligible for Somatic variant calls or for microsatellite instability processing. |
11 | isStranded* | This answer should be either "yes" or "no." |
12 | readPairOrientation* | Indicate the read pair orientation, such as forward or reverse. |
* optional but recommended
Whole Exome Sequencing
Annotation term | Additional Details | |
---|---|---|
1 | fileFormat | Accepted file formats include "fastq", "bam", and "cram". If provided raw data are “bam” or “cram” format, only files that have not undergone any additional filtering (i.e. retains unmapped reads, have not been trimmed, etc) will be eligible for processing. Note: WES files are not eligible for variant calling if BED file is not available |
2 | individualID | Individual IDs are necessary to create the sample sheets. |
3 | specimenID | specimen IDs are necessary to interpret the analysis. |
4 | Assay | Choose between Bulk RNA Seq or Single Cell RNA Seq. |
5 | Species | The corresponding genome requires knowledge of the species. |
6 | libraryPreparationMethod | This refers to the name of the library preparation, such as KAPA Hyper PCR 3. |
7 | Platform | This refers to the name of the platform used, for example, illumina. |
8 | readPair | Specify whether the read pair is 1 or 2. |
9 | specimenPreparationMethod | Minimize RNA degradation with methods such as flash freezing or RNALater. FFPE is not recommended. |
10 | tumorType | If the tissue is normal, indicate "not applicable." Otherwise, specify the tumor type. NOTE: Files from samples lacking tumor-normal pairs will not be eligible for Somatic variant calls or for microsatellite instability processing. |
11 | isStranded* | This answer should be either "yes" or "no." |
12 | readPairOrientation* | Indicate the read pair orientation, such as forward or reverse. |
* optional but recommended
Assay-specific workflow availability
The table below shows the availability of processing workflows for different data files generated through various ‘omics assays.
Assay | Germline SNV | Somatic SNV | Copy Number Variation (CNV) | Structural variants (SV) | Microsatellite Instability (MSI) | Raw counts |
WES | ✅ | ✅ | ✖️ | ✖️ | ✅ | |
WGS | ✅ | ✅ | ✅ | ✅ | ✅ | |
Bulk RNAseq | ✅ | |||||
Single Cell RNAseq | ✅ |
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