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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Detalles Bibliográficos
Autores principales: Cornish, Adam, Roychoudhury, Shrabasti, Sarma, Krishna, Pramanik, Suravi, Bhakat, Kishor, Dudley, Andrew, Mishra, Nitish K., Guda, Chittibabu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771073/
https://www.ncbi.nlm.nih.gov/pubmed/33372593
http://dx.doi.org/10.1186/s12864-020-07224-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771073/
https://www.ncbi.nlm.nih.gov/pubmed/33372593
http://dx.doi.org/10.1186/s12864-020-07224-3

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