URL: https://broadinstitute.github.io/warp/docs/Pipelines/scANVI_Pipeline/README
Proper Citation: scANVI pipeline (RRID:SCR_028705)
Description: Software cloud-optimized WDL workflow that performs cell type label transfer using scVI and scANVI (single-cell ANnotation using Variational Inference) deep generative models. It integrates single-cell RNA-seq (GEX) and, optionally, ATAC-seq data with an annotated reference dataset to transfer cell type labels via semi-supervised learning.
Synonyms: , single-cell ANnotation using Variational Inference
Resource Type: software resource, data processing software, software application, data analysis software
Keywords: Single-Cell ANnotation, variational inference, single cell data, 10x technology data, cell bar code correction pipeline, reads alignment, unique molecular identifier correction, mouse data sets analysis, human data sets analysis,
Expand AllWe found {{ ctrl2.mentions.all_count }} mentions in open access literature.
We have not found any literature mentions for this resource.
We are searching literature mentions for this resource.
Most recent articles:
{{ mention._source.dc.creators[0].familyName }} {{ mention._source.dc.creators[0].initials }}, et al. ({{ mention._source.dc.publicationYear }}) {{ mention._source.dc.title }} {{ mention._source.dc.publishers[0].name }}, {{ mention._source.dc.publishers[0].volume }}({{ mention._source.dc.publishers[0].issue }}), {{ mention._source.dc.publishers[0].pagination }}. (PMID:{{ mention._id.replace('PMID:', '') }})
A list of researchers who have used the resource and an author search tool
A list of researchers who have used the resource and an author search tool. This is available for resources that have literature mentions.
No rating or validation information has been found for scANVI pipeline.
No alerts have been found for scANVI pipeline.
Source: SciCrunch Registry