Skip to content

Commit

Permalink
mateStart etc
Browse files Browse the repository at this point in the history
  • Loading branch information
mbaudis committed Jul 25, 2024
1 parent 7bff882 commit 000b5ba
Showing 1 changed file with 75 additions and 1 deletion.
76 changes: 75 additions & 1 deletion src/config/beaconSearchParameters.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -5,11 +5,13 @@ parameters:
defaultValue: ["progenetix"]
options:
- value: progenetix
label: Progenetix
label: Progenetix cancer genome variants
- value: cellz
label: Cancer Cell Lines Collection
- value: examplez
label: Test Database - examplez
- value: refcnv
label: refCNV - germline reference CNVs
isMulti: true
assemblyId:
label: Genome Assembly
Expand Down Expand Up @@ -88,6 +90,60 @@ parameters:
value: "refseq:NC_000023.11"
- label: "Y (NC_000024.10)"
value: "refseq:NC_000024.10"
mateName:
label: Fusion Chromosome
infoText: The second chromosome in a fusion (transmitted as refseq id).
options:
- label: "(none)"
value: ""
- label: "1 (NC_000001.11)"
value: "refseq:NC_0000001.11"
- label: "2 (NC_000002.12)"
value: "refseq:NC_000002.12"
- label: "3 (NC_000003.12)"
value: "refseq:NC_000003.12"
- label: "4 (NC_000004.12)"
value: "refseq:NC_000004.12"
- label: "5 (NC_000005.10)"
value: "refseq:NC_000005.10"
- label: "6 (NC_000006.12)"
value: "refseq:NC_000006.12"
- label: "7 (NC_000007.14)"
value: "refseq:NC_000007.14"
- label: "8 (NC_000008.11)"
value: "refseq:NC_000008.11"
- label: "9 (NC_000009.12)"
value: "refseq:NC_000009.12"
- label: "10 (NC_000010.11)"
value: "refseq:NC_000010.11"
- label: "11 (NC_000011.10)"
value: "refseq:NC_000011.10"
- label: "12 (NC_000012.12)"
value: "refseq:NC_000012.12"
- label: "13 (NC_000013.11)"
value: "refseq:NC_000013.11"
- label: "14 (NC_000014.9)"
value: "refseq:NC_000014.9"
- label: "15 (NC_000015.10)"
value: "refseq:NC_000015.10"
- label: "16 (NC_000016.10)"
value: "refseq:NC_000016.10"
- label: "17 (NC_000017.11)"
value: "refseq:NC_000017.11"
- label: "18 (NC_000018.10)"
value: "refseq:NC_000018.10"
- label: "19 (NC_000019.10)"
value: "refseq:NC_000019.10"
- label: "20 (NC_000020.11)"
value: "refseq:NC_000020.11"
- label: "21 (NC_000021.9)"
value: "refseq:NC_000021.9"
- label: "22 (NC_000022.11)"
value: "refseq:NC_000022.11"
- label: "X (NC_000023.11)"
value: "refseq:NC_000023.11"
- label: "Y (NC_000024.10)"
value: "refseq:NC_000024.10"
variantType:
label: "Variant Type"
infoText: >-
Expand All @@ -108,6 +164,10 @@ parameters:
label: "EFO:0030066 (any relative CN variation)"
- value: "SO:0001059"
label: "SO:0001059 (any sequence alteration - SNV, INDEL...)"
- value: "SO:0000806"
label: "SO:0000806 (fusion)"
- value: "SO:0001413"
label: "SO:0001413 (translocation breakpoint)"
start:
label: Start or Position
placeholder: "19000001-21975098"
Expand All @@ -125,6 +185,20 @@ parameters:
single value, or in case of fuzzy requests for e.g. copy number variants
the end provided as a range for the possible occurrence of
the CNV end (e.g. "21967753-22500000").
mateStart:
label: Mate Start
placeholder: "23000000"
infoText: |
The (1-based) stat of genomic position of the range in which the fusion partners
breakpoint position should fall. In contrast to the general "start" parameter
only a single value can be used.
mateEnd:
label: Mate End
placeholder: "23000000"
infoText: |
The (1-based) stat of genomic position of the range in which the fusion partners
breakpoint position should fall. In contrast to the general "end" parameter
only a single value can be used.
cytoBands:
label: Cytoband Annotation
type: string
Expand Down

0 comments on commit 000b5ba

Please sign in to comment.