From 58cef7db5ebbba41589c605cd99e4c4c083c50cc Mon Sep 17 00:00:00 2001 From: "K. Joeri van der Velde" <82420+joerivandervelde@users.noreply.github.com> Date: Mon, 25 Sep 2023 14:58:15 +0200 Subject: [PATCH] Update resources --- generated/art-decor/fair-genomes_en-US.xml | 9 +++++ generated/latex/fair-genomes.tex | 6 ++-- .../markdown/fairgenomes-semantic-model.md | 6 ++-- ...amplepreparation_librarypreparationkit.tsv | 3 ++ .../samplepreparation_targetenrichmentkit.tsv | 3 ++ .../molgenis-emx2/librarypreparationkit.csv | 3 ++ .../molgenis-emx2/targetenrichmentkit.csv | 3 ++ generated/ontology/fair-genomes-ngskits.ttl | 35 +++++++++++++++++++ generated/palga-codebook/NGSKits.tsv | 3 ++ generated/resource/FG_0000747.xml | 19 ++++++++++ generated/resource/FG_0000748.xml | 19 ++++++++++ generated/resource/FG_0000749.xml | 19 ++++++++++ 12 files changed, 122 insertions(+), 6 deletions(-) create mode 100644 generated/resource/FG_0000747.xml create mode 100644 generated/resource/FG_0000748.xml create mode 100644 generated/resource/FG_0000749.xml diff --git a/generated/art-decor/fair-genomes_en-US.xml b/generated/art-decor/fair-genomes_en-US.xml index 1eeceb6..214f923 100644 --- a/generated/art-decor/fair-genomes_en-US.xml +++ b/generated/art-decor/fair-genomes_en-US.xml @@ -204160,6 +204160,15 @@ Options for Pre-filled, ready-to-use reagent cartridges intented to improve chem + + + + + + + + + diff --git a/generated/latex/fair-genomes.tex b/generated/latex/fair-genomes.tex index e09bf99..c1480b2 100644 --- a/generated/latex/fair-genomes.tex +++ b/generated/latex/fair-genomes.tex @@ -6,7 +6,7 @@ \textbf{FAIR Genomes metadata schema} \newline -The FAIR Genomes semantic metadata schema to power reuse of NGS data in research and healthcare. Version 1.3-SNAPSHOT, 2022-02-28. This model consists of 9 modules that contain 112 metadata elements and 85361 lookups in total (excluding null flavors). +The FAIR Genomes semantic metadata schema to power reuse of NGS data in research and healthcare. Version 1.3-SNAPSHOT, 2022-02-28. This model consists of 9 modules that contain 112 metadata elements and 85367 lookups in total (excluding null flavors). \begin{table}[htb] \begin{tabular}{lll} @@ -167,9 +167,9 @@ Sampleprep identifier & NCIT:C132299 & UniqueID \\ Belongs to material & NCIT:C25683 & Reference to Material \\ Input amount & AFRL:0000010 & Integer \\ -Library preparation kit & GENEPIO:0000085 & NGSKits lookup (616 choices) \\ +Library preparation kit & GENEPIO:0000085 & NGSKits lookup (619 choices) \\ PCR free & NCIT:C17003 & Boolean \\ -Target enrichment kit & NCIT:C154307 & NGSKits lookup (616 choices) \\ +Target enrichment kit & NCIT:C154307 & NGSKits lookup (619 choices) \\ UMIs present & EFO:0010199 & Boolean \\ Intended insert size & FG:0000001 & Integer \\ Intended read length & NCIT:C153362 & Integer \\ diff --git a/generated/markdown/fairgenomes-semantic-model.md b/generated/markdown/fairgenomes-semantic-model.md index ce39dd2..3bc9da3 100644 --- a/generated/markdown/fairgenomes-semantic-model.md +++ b/generated/markdown/fairgenomes-semantic-model.md @@ -1,6 +1,6 @@ # FAIR Genomes metadata schema -The FAIR Genomes semantic metadata schema to power reuse of NGS data in research and healthcare. Version 1.3-SNAPSHOT, 2022-02-28. This model consists of __9 modules__ that contain __112 metadata elements__ and __85361 lookups__ in total (excluding null flavors). +The FAIR Genomes semantic metadata schema to power reuse of NGS data in research and healthcare. Version 1.3-SNAPSHOT, 2022-02-28. This model consists of __9 modules__ that contain __112 metadata elements__ and __85367 lookups__ in total (excluding null flavors). ## Module overview @@ -140,9 +140,9 @@ A sample preparation for a nucleic acids sequencing assay. Ontology: [OBI:000190 | Sampleprep identifier | A unique proper name or character sequence that identifies this particular sample preparation. | [NCIT:C132299](http://purl.obolibrary.org/obo/NCIT_C132299) | UniqueID | | Belongs to material | Reference to the source material from which this sample was prepared. | [NCIT:C25683](http://purl.obolibrary.org/obo/NCIT_C25683) | Reference to instances of Material | | Input amount | Amount of input material in nanogram (ng). | [AFRL:0000010](http://purl.allotrope.org/ontologies/role#AFRL_0000010) | Integer | -| Library preparation kit | Pre-filled, ready-to-use reagent cartridges intented to improve chemistry, cluster density and read length as well as improve quality (Q) scores for this sample. Reagent components are encoded to interact with the sequencing system to validate compatibility with user-defined applications. | [GENEPIO:0000085](http://purl.obolibrary.org/obo/GENEPIO_0000085) | [NGSKits](../../lookups/NGSKits.txt) lookup (616 choices [of type](http://purl.obolibrary.org/obo/GENEPIO_0000081)) | +| Library preparation kit | Pre-filled, ready-to-use reagent cartridges intented to improve chemistry, cluster density and read length as well as improve quality (Q) scores for this sample. Reagent components are encoded to interact with the sequencing system to validate compatibility with user-defined applications. | [GENEPIO:0000085](http://purl.obolibrary.org/obo/GENEPIO_0000085) | [NGSKits](../../lookups/NGSKits.txt) lookup (619 choices [of type](http://purl.obolibrary.org/obo/GENEPIO_0000081)) | | PCR free | Indicates whether a polymerase chain reaction (PCR) was used to prepare this sample. PCR is a method for amplifying a DNA base sequence using multiple rounds of heat denaturation of the DNA and annealing of oligonucleotide primers complementary to flanking regions in the presence of a heat-stable polymerase. | [NCIT:C17003](http://purl.obolibrary.org/obo/NCIT_C17003) | Boolean | -| Target enrichment kit | Indicates which target enrichment kit was used to prepare this sample. Target enrichment is a pre-sequencing DNA preparation step where DNA sequences are either directly amplified (amplicon or multiplex PCR-based) or captured (hybrid capture-based) in order to only focus on specific regions of a genome or DNA sample. | [NCIT:C154307](http://purl.obolibrary.org/obo/NCIT_C154307) | [NGSKits](../../lookups/NGSKits.txt) lookup (616 choices [of type](http://purl.obolibrary.org/obo/GENEPIO_0000081)) | +| Target enrichment kit | Indicates which target enrichment kit was used to prepare this sample. Target enrichment is a pre-sequencing DNA preparation step where DNA sequences are either directly amplified (amplicon or multiplex PCR-based) or captured (hybrid capture-based) in order to only focus on specific regions of a genome or DNA sample. | [NCIT:C154307](http://purl.obolibrary.org/obo/NCIT_C154307) | [NGSKits](../../lookups/NGSKits.txt) lookup (619 choices [of type](http://purl.obolibrary.org/obo/GENEPIO_0000081)) | | UMIs present | Indicates whether any unique molecular identifiers (UMIs) are present. An UMI barcode is a short nucleotide sequence that is used to identify reads originating from an individual mRNA molecule. | [EFO:0010199](http://www.ebi.ac.uk/efo/EFO_0010199) | Boolean | | Intended insert size | In paired-end sequencing, the DNA between the adapter sequences is the insert. The length of this sequence is known as the insert size, not to be confused with the inner distance between reads. So, fragment length equals read adapter length (2x) plus insert size, and insert size equals read lenght (2x) plus inner distance. | [FG:0000001](https://w3id.org/fair-genomes/resource/FG_0000001) | Integer | | Intended read length | The number of nucleotides intended to be ordered from each side of a nucleic acid fragment obtained after the completion of a sequencing process. | [NCIT:C153362](http://purl.obolibrary.org/obo/NCIT_C153362) | Integer | diff --git a/generated/molgenis-emx/samplepreparation_librarypreparationkit.tsv b/generated/molgenis-emx/samplepreparation_librarypreparationkit.tsv index 389d738..9f3e08f 100644 --- a/generated/molgenis-emx/samplepreparation_librarypreparationkit.tsv +++ b/generated/molgenis-emx/samplepreparation_librarypreparationkit.tsv @@ -615,6 +615,9 @@ ClearSeq Inherited Disease Plus, 96, XT by Agilent Technologies ClearSeq Inherit ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020. FG 0000738 https://w3id.org/fair-genomes/resource/FG_0000738 ClearSeq Inherited Disease, 16, XT by Agilent Technologies ClearSeq Inherited Disease, 16, XT by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020. FG 0000739 https://w3id.org/fair-genomes/resource/FG_0000739 Illumina TruSeq DNA PCR-Free Illumina TruSeq DNA PCR-Free provides simple, all-inclusive library preparation for whole-genome sequencing applications. Illumina truseq-dna-pcr-free https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/truseq-dna-pcr-free.html +Accel-Amplicon Plus Panel by Swift Biosciences Accel-Amplicon Plus Panel by Swift Biosciences FG 0000747 https://w3id.org/fair-genomes/resource/FG_0000747 +TruSight Oncology 500 by Illumina TruSight Oncology 500 by Illumina FG 0000748 https://w3id.org/fair-genomes/resource/FG_0000748 +SeqCap EZ Choice Library SR by Roche NimbleGen SeqCap EZ Choice Library SR by Roche NimbleGen FG 0000749 https://w3id.org/fair-genomes/resource/FG_0000749 NoInformation (NI, nullflavor) The value is exceptional (missing, omitted, incomplete, improper). No information as to the reason for being an exceptional value is provided. This is the most general exceptional value. It is also the default exceptional value. HL7 NI http://terminology.hl7.org/CodeSystem/v3-NullFlavor#NI Invalid (INV, nullflavor) The value as represented in the instance is not a member of the set of permitted data values in the constrained value domain of a variable. HL7 INV http://terminology.hl7.org/CodeSystem/v3-NullFlavor#INV Derived (DER, nullflavor) An actual value may exist, but it must be derived from the provided information (usually an EXPR generic data type extension will be used to convey the derivation expression . HL7 DER http://terminology.hl7.org/CodeSystem/v3-NullFlavor#DER diff --git a/generated/molgenis-emx/samplepreparation_targetenrichmentkit.tsv b/generated/molgenis-emx/samplepreparation_targetenrichmentkit.tsv index 389d738..9f3e08f 100644 --- a/generated/molgenis-emx/samplepreparation_targetenrichmentkit.tsv +++ b/generated/molgenis-emx/samplepreparation_targetenrichmentkit.tsv @@ -615,6 +615,9 @@ ClearSeq Inherited Disease Plus, 96, XT by Agilent Technologies ClearSeq Inherit ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020. FG 0000738 https://w3id.org/fair-genomes/resource/FG_0000738 ClearSeq Inherited Disease, 16, XT by Agilent Technologies ClearSeq Inherited Disease, 16, XT by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020. FG 0000739 https://w3id.org/fair-genomes/resource/FG_0000739 Illumina TruSeq DNA PCR-Free Illumina TruSeq DNA PCR-Free provides simple, all-inclusive library preparation for whole-genome sequencing applications. Illumina truseq-dna-pcr-free https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/truseq-dna-pcr-free.html +Accel-Amplicon Plus Panel by Swift Biosciences Accel-Amplicon Plus Panel by Swift Biosciences FG 0000747 https://w3id.org/fair-genomes/resource/FG_0000747 +TruSight Oncology 500 by Illumina TruSight Oncology 500 by Illumina FG 0000748 https://w3id.org/fair-genomes/resource/FG_0000748 +SeqCap EZ Choice Library SR by Roche NimbleGen SeqCap EZ Choice Library SR by Roche NimbleGen FG 0000749 https://w3id.org/fair-genomes/resource/FG_0000749 NoInformation (NI, nullflavor) The value is exceptional (missing, omitted, incomplete, improper). No information as to the reason for being an exceptional value is provided. This is the most general exceptional value. It is also the default exceptional value. HL7 NI http://terminology.hl7.org/CodeSystem/v3-NullFlavor#NI Invalid (INV, nullflavor) The value as represented in the instance is not a member of the set of permitted data values in the constrained value domain of a variable. HL7 INV http://terminology.hl7.org/CodeSystem/v3-NullFlavor#INV Derived (DER, nullflavor) An actual value may exist, but it must be derived from the provided information (usually an EXPR generic data type extension will be used to convey the derivation expression . HL7 DER http://terminology.hl7.org/CodeSystem/v3-NullFlavor#DER diff --git a/generated/molgenis-emx2/librarypreparationkit.csv b/generated/molgenis-emx2/librarypreparationkit.csv index f5e05ae..1f90e73 100644 --- a/generated/molgenis-emx2/librarypreparationkit.csv +++ b/generated/molgenis-emx2/librarypreparationkit.csv @@ -615,6 +615,9 @@ name,definition,codesystem,code,ontologyTermURI "ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies","ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020.","FG","0000738","https://w3id.org/fair-genomes/resource/FG_0000738" "ClearSeq Inherited Disease, 16, XT by Agilent Technologies","ClearSeq Inherited Disease, 16, XT by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020.","FG","0000739","https://w3id.org/fair-genomes/resource/FG_0000739" "Illumina TruSeq DNA PCR-Free","Illumina TruSeq DNA PCR-Free provides simple, all-inclusive library preparation for whole-genome sequencing applications.","Illumina","truseq-dna-pcr-free","https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/truseq-dna-pcr-free.html" +"Accel-Amplicon Plus Panel by Swift Biosciences","Accel-Amplicon Plus Panel by Swift Biosciences","FG","0000747","https://w3id.org/fair-genomes/resource/FG_0000747" +"TruSight Oncology 500 by Illumina","TruSight Oncology 500 by Illumina","FG","0000748","https://w3id.org/fair-genomes/resource/FG_0000748" +"SeqCap EZ Choice Library SR by Roche NimbleGen","SeqCap EZ Choice Library SR by Roche NimbleGen","FG","0000749","https://w3id.org/fair-genomes/resource/FG_0000749" "NoInformation (NI, nullflavor)","The value is exceptional (missing, omitted, incomplete, improper). No information as to the reason for being an exceptional value is provided. This is the most general exceptional value. It is also the default exceptional value.","HL7","NI","http://terminology.hl7.org/CodeSystem/v3-NullFlavor#NI" "Invalid (INV, nullflavor)","The value as represented in the instance is not a member of the set of permitted data values in the constrained value domain of a variable.","HL7","INV","http://terminology.hl7.org/CodeSystem/v3-NullFlavor#INV" "Derived (DER, nullflavor)","An actual value may exist, but it must be derived from the provided information (usually an EXPR generic data type extension will be used to convey the derivation expression .","HL7","DER","http://terminology.hl7.org/CodeSystem/v3-NullFlavor#DER" diff --git a/generated/molgenis-emx2/targetenrichmentkit.csv b/generated/molgenis-emx2/targetenrichmentkit.csv index f5e05ae..1f90e73 100644 --- a/generated/molgenis-emx2/targetenrichmentkit.csv +++ b/generated/molgenis-emx2/targetenrichmentkit.csv @@ -615,6 +615,9 @@ name,definition,codesystem,code,ontologyTermURI "ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies","ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020.","FG","0000738","https://w3id.org/fair-genomes/resource/FG_0000738" "ClearSeq Inherited Disease, 16, XT by Agilent Technologies","ClearSeq Inherited Disease, 16, XT by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020.","FG","0000739","https://w3id.org/fair-genomes/resource/FG_0000739" "Illumina TruSeq DNA PCR-Free","Illumina TruSeq DNA PCR-Free provides simple, all-inclusive library preparation for whole-genome sequencing applications.","Illumina","truseq-dna-pcr-free","https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/truseq-dna-pcr-free.html" +"Accel-Amplicon Plus Panel by Swift Biosciences","Accel-Amplicon Plus Panel by Swift Biosciences","FG","0000747","https://w3id.org/fair-genomes/resource/FG_0000747" +"TruSight Oncology 500 by Illumina","TruSight Oncology 500 by Illumina","FG","0000748","https://w3id.org/fair-genomes/resource/FG_0000748" +"SeqCap EZ Choice Library SR by Roche NimbleGen","SeqCap EZ Choice Library SR by Roche NimbleGen","FG","0000749","https://w3id.org/fair-genomes/resource/FG_0000749" "NoInformation (NI, nullflavor)","The value is exceptional (missing, omitted, incomplete, improper). No information as to the reason for being an exceptional value is provided. This is the most general exceptional value. It is also the default exceptional value.","HL7","NI","http://terminology.hl7.org/CodeSystem/v3-NullFlavor#NI" "Invalid (INV, nullflavor)","The value as represented in the instance is not a member of the set of permitted data values in the constrained value domain of a variable.","HL7","INV","http://terminology.hl7.org/CodeSystem/v3-NullFlavor#INV" "Derived (DER, nullflavor)","An actual value may exist, but it must be derived from the provided information (usually an EXPR generic data type extension will be used to convey the derivation expression .","HL7","DER","http://terminology.hl7.org/CodeSystem/v3-NullFlavor#DER" diff --git a/generated/ontology/fair-genomes-ngskits.ttl b/generated/ontology/fair-genomes-ngskits.ttl index c195481..fd096bb 100644 --- a/generated/ontology/fair-genomes-ngskits.ttl +++ b/generated/ontology/fair-genomes-ngskits.ttl @@ -3692,6 +3692,24 @@ fg:Sample_preparation_Library_preparation_kit_Illumina_TruSeq_DNA_PCR-Free a obo dc:description "Illumina TruSeq DNA PCR-Free provides simple, all-inclusive library preparation for whole-genome sequencing applications."; rdfs:isDefinedBy . +fg:Sample_preparation_Library_preparation_kit_Accel-Amplicon_Plus_Panel_by_Swift_Biosciences + a obo:GENEPIO_0000081; + rdfs:label "Accel-Amplicon Plus Panel by Swift Biosciences"; + dc:description "Accel-Amplicon Plus Panel by Swift Biosciences"; + rdfs:isDefinedBy . + +fg:Sample_preparation_Library_preparation_kit_TruSight_Oncology_500_by_Illumina a + obo:GENEPIO_0000081; + rdfs:label "TruSight Oncology 500 by Illumina"; + dc:description "TruSight Oncology 500 by Illumina"; + rdfs:isDefinedBy . + +fg:Sample_preparation_Library_preparation_kit_SeqCap_EZ_Choice_Library_SR_by_Roche_NimbleGen + a obo:GENEPIO_0000081; + rdfs:label "SeqCap EZ Choice Library SR by Roche NimbleGen"; + dc:description "SeqCap EZ Choice Library SR by Roche NimbleGen"; + rdfs:isDefinedBy . + a obo:GENEPIO_0000081; rdfs:label "NoInformation (NI, nullflavor)"; @@ -7470,6 +7488,23 @@ fg:Sample_preparation_Target_enrichment_kit_Illumina_TruSeq_DNA_PCR-Free a obo:G dc:description "Illumina TruSeq DNA PCR-Free provides simple, all-inclusive library preparation for whole-genome sequencing applications."; rdfs:isDefinedBy . +fg:Sample_preparation_Target_enrichment_kit_Accel-Amplicon_Plus_Panel_by_Swift_Biosciences + a obo:GENEPIO_0000081; + rdfs:label "Accel-Amplicon Plus Panel by Swift Biosciences"; + dc:description "Accel-Amplicon Plus Panel by Swift Biosciences"; + rdfs:isDefinedBy . + +fg:Sample_preparation_Target_enrichment_kit_TruSight_Oncology_500_by_Illumina a obo:GENEPIO_0000081; + rdfs:label "TruSight Oncology 500 by Illumina"; + dc:description "TruSight Oncology 500 by Illumina"; + rdfs:isDefinedBy . + +fg:Sample_preparation_Target_enrichment_kit_SeqCap_EZ_Choice_Library_SR_by_Roche_NimbleGen + a obo:GENEPIO_0000081; + rdfs:label "SeqCap EZ Choice Library SR by Roche NimbleGen"; + dc:description "SeqCap EZ Choice Library SR by Roche NimbleGen"; + rdfs:isDefinedBy . + a obo:GENEPIO_0000081; rdfs:label "NoInformation (NI, nullflavor)"; diff --git a/generated/palga-codebook/NGSKits.tsv b/generated/palga-codebook/NGSKits.tsv index 1ba759a..e7dd1ef 100644 --- a/generated/palga-codebook/NGSKits.tsv +++ b/generated/palga-codebook/NGSKits.tsv @@ -615,6 +615,9 @@ ClearSeq Inherited Disease Plus, 96, XT by Agilent Technologies ClearSeq Inherit ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020. FG https://w3id.org/fair-genomes/resource/FG_0000738 ClearSeq Inherited Disease Plus, 96, XT2 by Agilent Technologies ClearSeq Inherited Disease, 16, XT by Agilent Technologies ClearSeq Inherited Disease, 16, XT by Agilent Technologies sourced from https://www.biocompare.com, accessed May 2020. FG https://w3id.org/fair-genomes/resource/FG_0000739 ClearSeq Inherited Disease, 16, XT by Agilent Technologies Illumina TruSeq DNA PCR-Free Illumina TruSeq DNA PCR-Free provides simple, all-inclusive library preparation for whole-genome sequencing applications. Illumina https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/truseq-dna-pcr-free.html Illumina TruSeq DNA PCR-Free +Accel-Amplicon Plus Panel by Swift Biosciences Accel-Amplicon Plus Panel by Swift Biosciences FG https://w3id.org/fair-genomes/resource/FG_0000747 Accel-Amplicon Plus Panel by Swift Biosciences +TruSight Oncology 500 by Illumina TruSight Oncology 500 by Illumina FG https://w3id.org/fair-genomes/resource/FG_0000748 TruSight Oncology 500 by Illumina +SeqCap EZ Choice Library SR by Roche NimbleGen SeqCap EZ Choice Library SR by Roche NimbleGen FG https://w3id.org/fair-genomes/resource/FG_0000749 SeqCap EZ Choice Library SR by Roche NimbleGen NoInformation (NI, nullflavor) The value is exceptional (missing, omitted, incomplete, improper). No information as to the reason for being an exceptional value is provided. This is the most general exceptional value. It is also the default exceptional value. HL7 http://terminology.hl7.org/CodeSystem/v3-NullFlavor#NI NoInformation (NI, nullflavor) Invalid (INV, nullflavor) The value as represented in the instance is not a member of the set of permitted data values in the constrained value domain of a variable. HL7 http://terminology.hl7.org/CodeSystem/v3-NullFlavor#INV Invalid (INV, nullflavor) Derived (DER, nullflavor) An actual value may exist, but it must be derived from the provided information (usually an EXPR generic data type extension will be used to convey the derivation expression . HL7 http://terminology.hl7.org/CodeSystem/v3-NullFlavor#DER Derived (DER, nullflavor) diff --git a/generated/resource/FG_0000747.xml b/generated/resource/FG_0000747.xml new file mode 100644 index 0000000..360db44 --- /dev/null +++ b/generated/resource/FG_0000747.xml @@ -0,0 +1,19 @@ + + + + + + + + Accel-Amplicon Plus Panel by Swift Biosciences + + Accel-Amplicon Plus Panel by Swift Biosciences + FG:0000747 + FG_0000747 + + + diff --git a/generated/resource/FG_0000748.xml b/generated/resource/FG_0000748.xml new file mode 100644 index 0000000..f6e7b63 --- /dev/null +++ b/generated/resource/FG_0000748.xml @@ -0,0 +1,19 @@ + + + + + + + + TruSight Oncology 500 by Illumina + + TruSight Oncology 500 by Illumina + FG:0000748 + FG_0000748 + + + diff --git a/generated/resource/FG_0000749.xml b/generated/resource/FG_0000749.xml new file mode 100644 index 0000000..0c16ca1 --- /dev/null +++ b/generated/resource/FG_0000749.xml @@ -0,0 +1,19 @@ + + + + + + + + SeqCap EZ Choice Library SR by Roche NimbleGen + + SeqCap EZ Choice Library SR by Roche NimbleGen + FG:0000749 + FG_0000749 + + +