Browse Wiki & Semantic Web

Jump to: navigation, search
Http://dbpedia.org/resource/Perturb-seq
  This page has no properties.
hide properties that link here 
  No properties link to this page.
 
http://dbpedia.org/resource/Perturb-seq
http://dbpedia.org/ontology/abstract Perturb-seq (also known as CRISP-seq and CPerturb-seq (also known as CRISP-seq and CROP-seq) refers to a high-throughput method of performing single cell RNA sequencing (scRNA-seq) on pooled genetic perturbation screens. Perturb-seq combines multiplexed CRISPR mediated gene inactivations with single cell RNA sequencing to assess comprehensive gene expression phenotypes for each perturbation. Inferring a gene’s function by applying genetic perturbations to knock down or knock out a gene and studying the resulting phenotype is known as reverse genetics. Perturb-seq is a reverse genetics approach that allows for the investigation of phenotypes at the level of the transcriptome, to elucidate gene functions in many cells, in a massively parallel fashion. The Perturb-seq protocol uses CRISPR technology to inactivate specific genes and DNA barcoding of each guide RNA to allow for all perturbations to be pooled together and later deconvoluted, with assignment of each phenotype to a specific guide RNA. Droplet-based microfluidics platforms (or other cell sorting and separating techniques) are used to isolate individual cells, and then scRNA-seq is performed to generate gene expression profiles for each cell. Upon completion of the protocol, bioinformatics analyses are conducted to associate each specific cell and perturbation with a transcriptomic profile that characterizes the consequences of inactivating each gene.he consequences of inactivating each gene.
http://dbpedia.org/ontology/thumbnail http://commons.wikimedia.org/wiki/Special:FilePath/Overview_of_Perturb-seq_workflow.jpeg?width=300 +
http://dbpedia.org/ontology/wikiPageID 53353992
http://dbpedia.org/ontology/wikiPageLength 20042
http://dbpedia.org/ontology/wikiPageRevisionID 1120612919
http://dbpedia.org/ontology/wikiPageWikiLink http://dbpedia.org/resource/Cell_%28journal%29 + , http://dbpedia.org/resource/Lentiviral_vector_in_gene_therapy + , http://dbpedia.org/resource/Immune_response + , http://dbpedia.org/resource/Library_%28biology%29 + , http://dbpedia.org/resource/Zinc_finger_nuclease + , http://dbpedia.org/resource/Microfluidics + , http://dbpedia.org/resource/Jurkat_cells + , http://dbpedia.org/resource/Antimicrobial_resistance + , http://dbpedia.org/resource/Single_cell_sequencing + , http://dbpedia.org/resource/Reverse_genetics + , http://dbpedia.org/resource/Gene_expression + , http://dbpedia.org/resource/Category:Molecular_biology_techniques + , http://dbpedia.org/resource/Phenotype + , http://dbpedia.org/resource/CRISPR_interference + , http://dbpedia.org/resource/CRISPR + , http://dbpedia.org/resource/RNA_interference + , http://dbpedia.org/resource/Phenotypes + , http://dbpedia.org/resource/Multiplicity_of_Infection + , http://dbpedia.org/resource/Promoter_%28genetics%29 + , http://dbpedia.org/resource/Unique_molecular_identifiers + , http://dbpedia.org/resource/Nature_Methods + , http://dbpedia.org/resource/Machine_learning + , http://dbpedia.org/resource/Nuclease + , http://dbpedia.org/resource/Category:Bioinformatics + , http://dbpedia.org/resource/CRISPR/Cas_Tools + , http://dbpedia.org/resource/Reverse_transcription + , http://dbpedia.org/resource/Transduction_%28genetics%29 + , http://dbpedia.org/resource/Forward_genetics + , http://dbpedia.org/resource/T-distributed_stochastic_neighbor_embedding + , http://dbpedia.org/resource/Cell_cycle + , http://dbpedia.org/resource/File:Overview_of_Perturb-seq_workflow.jpeg + , http://dbpedia.org/resource/Category:Genomics + , http://dbpedia.org/resource/BioRxiv + , http://dbpedia.org/resource/Transcription_factors + , http://dbpedia.org/resource/Innate_immune_system + , http://dbpedia.org/resource/Restriction_sites + , http://dbpedia.org/resource/Reporter_gene + , http://dbpedia.org/resource/Bioinformatics + , http://dbpedia.org/resource/Gene_knockout + , http://dbpedia.org/resource/Transcription_%28genetics%29 + , http://dbpedia.org/resource/Non-homologous_end_joining + , http://dbpedia.org/resource/Epistasis_and_functional_genomics + , http://dbpedia.org/resource/Transcription_activator-like_effector_nuclease + , http://dbpedia.org/resource/Primer_%28molecular_biology%29 + , http://dbpedia.org/resource/DNA_barcoding + , http://dbpedia.org/resource/Gene_knockdown + , http://dbpedia.org/resource/UCSF + , http://dbpedia.org/resource/Cpf1 + , http://dbpedia.org/resource/Category:RNA_sequencing + , http://dbpedia.org/resource/RNA_polymerase + , http://dbpedia.org/resource/Cas9 + , http://dbpedia.org/resource/Unfolded_protein_response + , http://dbpedia.org/resource/Transcriptome +
http://dbpedia.org/property/wikiPageUsesTemplate http://dbpedia.org/resource/Template:Reflist +
http://purl.org/dc/terms/subject http://dbpedia.org/resource/Category:RNA_sequencing + , http://dbpedia.org/resource/Category:Bioinformatics + , http://dbpedia.org/resource/Category:Molecular_biology_techniques + , http://dbpedia.org/resource/Category:Genomics +
http://www.w3.org/ns/prov#wasDerivedFrom http://en.wikipedia.org/wiki/Perturb-seq?oldid=1120612919&ns=0 +
http://xmlns.com/foaf/0.1/depiction http://commons.wikimedia.org/wiki/Special:FilePath/Overview_of_Perturb-seq_workflow.jpeg +
http://xmlns.com/foaf/0.1/isPrimaryTopicOf http://en.wikipedia.org/wiki/Perturb-seq +
owl:sameAs http://yago-knowledge.org/resource/Perturb-seq + , http://www.wikidata.org/entity/Q30314275 + , https://global.dbpedia.org/id/2ogr4 + , http://dbpedia.org/resource/Perturb-seq +
rdfs:comment Perturb-seq (also known as CRISP-seq and CPerturb-seq (also known as CRISP-seq and CROP-seq) refers to a high-throughput method of performing single cell RNA sequencing (scRNA-seq) on pooled genetic perturbation screens. Perturb-seq combines multiplexed CRISPR mediated gene inactivations with single cell RNA sequencing to assess comprehensive gene expression phenotypes for each perturbation. Inferring a gene’s function by applying genetic perturbations to knock down or knock out a gene and studying the resulting phenotype is known as reverse genetics. Perturb-seq is a reverse genetics approach that allows for the investigation of phenotypes at the level of the transcriptome, to elucidate gene functions in many cells, in a massively parallel fashion.ny cells, in a massively parallel fashion.
rdfs:label Perturb-seq
hide properties that link here 
http://dbpedia.org/resource/Overlapping_gene + http://dbpedia.org/ontology/wikiPageWikiLink
http://en.wikipedia.org/wiki/Perturb-seq + http://xmlns.com/foaf/0.1/primaryTopic
http://dbpedia.org/resource/Perturb-seq + owl:sameAs
 

 

Enter the name of the page to start semantic browsing from.