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on page 1 showing 20 out of 597 results from 1 sources
http://web.expasy.org/cellosaurus/CVCL_0617

Cite this ATCC Cat# HTB-23, RRID:CVCL_0617
Organism: Homo sapiens
Disease: Invasive lobular breast carcinoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: FGFR genetic alteration cell panel (ATCC TCP-1034). Part of: ICBP43 breast cancer cell line panel. Part of: MD Anderson Cell Lines Project. Doubling time: 6.4 days (PubMed=9671407). Omics: CNV analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: miRNA expression profiling. Omics: Protein expression by reverse-phase protein arrays. Omics: SNP array analysis. Omics: Transcriptome analysis. Misspelling: 'MDA-MB-134IV' in Cosmic 1000129. Misspelling: 'MDA-MB-134-IV' in Cosmic 1090333. Derived from metastatic site: Pleural effusion.

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http://web.expasy.org/cellosaurus/CVCL_0620

Cite this ATCC Cat# HTB-27, RRID:CVCL_0620
Organism: Homo sapiens
Disease: Breast adenocarcinoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: EGFR genetic alteration cell panel (ATCC TCP-1027). Part of: ICBP43 breast cancer cell line panel. Part of: KuDOS 95 cell line panel. Part of: MD Anderson Cell Lines Project. Part of: PI3K genetic alteration cell panel (ATCC TCP-1028). Doubling time: 4.3 days (PubMed=9671407). Microsatellite instability: Stable (MSS) (Sanger). Omics: Array-based CGH. Omics: CNV analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: miRNA expression profiling. Omics: Protein expression by reverse-phase protein arrays. Omics: SNP array analysis. Omics: Transcriptome analysis. Derived from metastatic site: Brain.

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http://web.expasy.org/cellosaurus/CVCL_0020

Cite this CLS Cat# 300363/p511_U-138_MG, RRID:CVCL_0020
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Doubling time: ~70 hours (DSMZ). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep RNAseq analysis. Omics: SNP array analysis. Omics: Transcriptome analysis.

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http://web.expasy.org/cellosaurus/CVCL_0023

Cite this DSMZ Cat# ACC-107, RRID:CVCL_0023
Organism: Homo sapiens
Disease: Lung adenocarcinoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: ENCODE project common cell types; tier 2. Part of: JFCR39 cancer cell line panel. Part of: KuDOS 95 cell line panel. Part of: MD Anderson Cell Lines Project. Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982). Part of: NCI60 cancer cell line panel. Doubling time: 18 hours (in RPMI 1640+10% FBS), 37 hours (in ACL-3), 36 hours (in ACL-3+BSA) (PubMed=3940644); 22 hours (PubMed=25984343); 27 hours (from cell counting), 27 hours (from absorbance) (DOI=10.5897/IJBMBR2013.0154); 22.9 hours (NCI-DTP); ~40 hours (DSMZ). Microsatellite instability: Stable (MSS) (PubMed=12661003; Sanger). Sequence variation: Homozygous for KRAS p.Gly12Ser (PubMed=17088437). Sequence variation: Homozygous for STK11 p.Gln37Ter (PubMed=17088437). Omics: Acetylation analysis by proteomics. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep phosphoproteome analysis. Omics: Deep membrane proteome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: H3K4me3 ChIP-seq epigenome analysis. Omics: H3K9ac ChIP-seq epigenome analysis. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: Proteome analysis by 2D-DE/MS. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Omics: Virome analysis using proteomics. Misspelling: 'A594' in PubMed=18227028. Misspelling: 'A59' in PubMed=16354588. Discontinued: ATCC; CRL-7909.

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http://web.expasy.org/cellosaurus/CVCL_0020

Cite this BCRJ Cat# 0239, RRID:CVCL_0020
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Doubling time: ~70 hours (DSMZ). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep RNAseq analysis. Omics: SNP array analysis. Omics: Transcriptome analysis.

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http://web.expasy.org/cellosaurus/CVCL_0020

Cite this DSMZ Cat# ACC-291, RRID:CVCL_0020
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Doubling time: ~70 hours (DSMZ). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep RNAseq analysis. Omics: SNP array analysis. Omics: Transcriptome analysis.

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http://web.expasy.org/cellosaurus/CVCL_0020

Cite this ATCC Cat# HTB-16, RRID:CVCL_0020
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Doubling time: ~70 hours (DSMZ). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep RNAseq analysis. Omics: SNP array analysis. Omics: Transcriptome analysis.

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http://web.expasy.org/cellosaurus/CVCL_0021

Cite this IFO Cat# IFO50288, RRID:CVCL_0021
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: JFCR39 cancer cell line panel. Part of: MD Anderson Cell Lines Project. Part of: NCI60 cancer cell line panel. Doubling time: 24 hours (PubMed=25984343); 23.8 hours (NCI-DTP). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0461.

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http://web.expasy.org/cellosaurus/CVCL_0021

Cite this RCB Cat# RCB0461, RRID:CVCL_0021
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: JFCR39 cancer cell line panel. Part of: MD Anderson Cell Lines Project. Part of: NCI60 cancer cell line panel. Doubling time: 24 hours (PubMed=25984343); 23.8 hours (NCI-DTP). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0461.

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http://web.expasy.org/cellosaurus/CVCL_0021

Cite this ECACC Cat# 09063001, RRID:CVCL_0021
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: JFCR39 cancer cell line panel. Part of: MD Anderson Cell Lines Project. Part of: NCI60 cancer cell line panel. Doubling time: 24 hours (PubMed=25984343); 23.8 hours (NCI-DTP). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0461.

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http://web.expasy.org/cellosaurus/CVCL_0021

Cite this NCI-DTP Cat# U-251, RRID:CVCL_0021
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: JFCR39 cancer cell line panel. Part of: MD Anderson Cell Lines Project. Part of: NCI60 cancer cell line panel. Doubling time: 24 hours (PubMed=25984343); 23.8 hours (NCI-DTP). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0461.

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http://web.expasy.org/cellosaurus/CVCL_0021

Cite this ICLC Cat# HTL99014, RRID:CVCL_0021
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: JFCR39 cancer cell line panel. Part of: MD Anderson Cell Lines Project. Part of: NCI60 cancer cell line panel. Doubling time: 24 hours (PubMed=25984343); 23.8 hours (NCI-DTP). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0461.

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http://web.expasy.org/cellosaurus/CVCL_0023

Cite this ATCC Cat# CRL-7909, RRID:CVCL_0023
Organism: Homo sapiens
Disease: Lung adenocarcinoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: ENCODE project common cell types; tier 2. Part of: JFCR39 cancer cell line panel. Part of: KuDOS 95 cell line panel. Part of: MD Anderson Cell Lines Project. Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982). Part of: NCI60 cancer cell line panel. Doubling time: 18 hours (in RPMI 1640+10% FBS), 37 hours (in ACL-3), 36 hours (in ACL-3+BSA) (PubMed=3940644); 22 hours (PubMed=25984343); 27 hours (from cell counting), 27 hours (from absorbance) (DOI=10.5897/IJBMBR2013.0154); 22.9 hours (NCI-DTP); ~40 hours (DSMZ). Microsatellite instability: Stable (MSS) (PubMed=12661003; Sanger). Sequence variation: Homozygous for KRAS p.Gly12Ser (PubMed=17088437). Sequence variation: Homozygous for STK11 p.Gln37Ter (PubMed=17088437). Omics: Acetylation analysis by proteomics. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep phosphoproteome analysis. Omics: Deep membrane proteome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: H3K4me3 ChIP-seq epigenome analysis. Omics: H3K9ac ChIP-seq epigenome analysis. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: Proteome analysis by 2D-DE/MS. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Omics: Virome analysis using proteomics. Misspelling: 'A594' in PubMed=18227028. Misspelling: 'A59' in PubMed=16354588. Discontinued: ATCC; CRL-7909.

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http://web.expasy.org/cellosaurus/CVCL_0021

Cite this CLS Cat# 300385/p534_U251_MG, RRID:CVCL_0021
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: JFCR39 cancer cell line panel. Part of: MD Anderson Cell Lines Project. Part of: NCI60 cancer cell line panel. Doubling time: 24 hours (PubMed=25984343); 23.8 hours (NCI-DTP). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0461.

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http://web.expasy.org/cellosaurus/CVCL_0021

Cite this KCB Cat# KCB 200965YJ, RRID:CVCL_0021
Organism: Homo sapiens
Disease: Astrocytoma
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: JFCR39 cancer cell line panel. Part of: MD Anderson Cell Lines Project. Part of: NCI60 cancer cell line panel. Doubling time: 24 hours (PubMed=25984343); 23.8 hours (NCI-DTP). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0461.

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http://web.expasy.org/cellosaurus/CVCL_0022

Cite this KCLB Cat# 30014, RRID:CVCL_0022
Organism: Homo sapiens
Disease: Glioblastoma
Category: Cancer cell line
Comment: Problematic cell line: Contaminated/misidentified. This cell line is not the original glioblastoma cell line established in 1968 at the University of Uppsala. As described in PubMed=27582061 it is most probably also a glioblastoma cell line but whose origin is unknow. See U-87MG Uppsala (CVCL_GP63) for the original U-87MG cell line. Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: ENCODE project common cell types; tier 3. Doubling time: 72 hours (PubMed=25984343). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Genome sequenced. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0419.

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http://web.expasy.org/cellosaurus/CVCL_0022

Cite this NCBI_Iran Cat# C531, RRID:CVCL_0022
Organism: Homo sapiens
Disease: Glioblastoma
Category: Cancer cell line
Comment: Problematic cell line: Contaminated/misidentified. This cell line is not the original glioblastoma cell line established in 1968 at the University of Uppsala. As described in PubMed=27582061 it is most probably also a glioblastoma cell line but whose origin is unknow. See U-87MG Uppsala (CVCL_GP63) for the original U-87MG cell line. Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: ENCODE project common cell types; tier 3. Doubling time: 72 hours (PubMed=25984343). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Genome sequenced. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0419.

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http://web.expasy.org/cellosaurus/CVCL_0022

Cite this NIH-ARP Cat# 2188-324, RRID:CVCL_0022
Organism: Homo sapiens
Disease: Glioblastoma
Category: Cancer cell line
Comment: Problematic cell line: Contaminated/misidentified. This cell line is not the original glioblastoma cell line established in 1968 at the University of Uppsala. As described in PubMed=27582061 it is most probably also a glioblastoma cell line but whose origin is unknow. See U-87MG Uppsala (CVCL_GP63) for the original U-87MG cell line. Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: ENCODE project common cell types; tier 3. Doubling time: 72 hours (PubMed=25984343). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Genome sequenced. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0419.

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http://web.expasy.org/cellosaurus/CVCL_0022

Cite this BCRC Cat# 60360, RRID:CVCL_0022
Organism: Homo sapiens
Disease: Glioblastoma
Category: Cancer cell line
Comment: Problematic cell line: Contaminated/misidentified. This cell line is not the original glioblastoma cell line established in 1968 at the University of Uppsala. As described in PubMed=27582061 it is most probably also a glioblastoma cell line but whose origin is unknow. See U-87MG Uppsala (CVCL_GP63) for the original U-87MG cell line. Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: ENCODE project common cell types; tier 3. Doubling time: 72 hours (PubMed=25984343). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Genome sequenced. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0419.

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http://web.expasy.org/cellosaurus/CVCL_0022

Cite this ATCC Cat# HTB-14, RRID:CVCL_0022
Organism: Homo sapiens
Disease: Glioblastoma
Category: Cancer cell line
Comment: Problematic cell line: Contaminated/misidentified. This cell line is not the original glioblastoma cell line established in 1968 at the University of Uppsala. As described in PubMed=27582061 it is most probably also a glioblastoma cell line but whose origin is unknow. See U-87MG Uppsala (CVCL_GP63) for the original U-87MG cell line. Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: ENCODE project common cell types; tier 3. Doubling time: 72 hours (PubMed=25984343). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Has no IDH1 mutation (PubMed=19435942). Omics: Cell surface proteome. Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Genome sequenced. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: RCB; RCB0419.

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