Red panda: a novel method for detecting variants in single-cell RNA sequencing

BACKGROUND: Single-cell sequencing enables us to better understand genetic diseases, such as cancer or autoimmune disorders, which are often affected by changes in rare cells. Currently, no existing software is aimed at identifying single nucleotide variations or micro (1-50 bp) insertions and delet...

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Detalhes bibliográficos
Publicado no:BMC Genomics
Main Authors: Cornish, Adam, Roychoudhury, Shrabasti, Sarma, Krishna, Pramanik, Suravi, Bhakat, Kishor, Dudley, Andrew, Mishra, Nitish K., Guda, Chittibabu
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7771073/
https://ncbi.nlm.nih.gov/pubmed/33372593
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-020-07224-3
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