A validated pipeline for detection of SNVs and short InDels from RNA Sequencing
Effective identification of genomic variations is a crucial step to understand the relationship between genotype and phenotype and it can yield important insights into rare diseases and cancer biology. Exome and whole-genome sequencing are now routinely used in clinics for detection of disease causi...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Science Planet Inc.
2017-12-01
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| Series: | Canadian Journal of Biotechnology |
| Online Access: | https://www.canadianjbiotech.com/CAN_J_BIOTECH/Archives/v1/Special Issue-Supplement/cjb.2017-a210.pdf |