This information is over 2 years old.
Information was current at time of publication.
This information is over 2 years old.
Information was current at time of publication.
WHEN: August 2nd, 1-4 pm
WHERE: Falk Library, Classroom 2
WHO: Ansuman Chattopadhyay, PhD
Information was current at time of publication.
Researchers have been finding variants and mutations using Sequencher software for a long time. Sequencher’s powerful algorithms and ease of use have made it a staple for genetic researchers all over the world. One of the earliest studies linking the Human Mutator Gene Homolog MSH2 to colon cancer featured Sequencher as the software of choice.
Information was current at time of publication.
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Massively parallel RNA sequencing, commonly known as RNA-seq, provides a more detailed picture of transcriptomes compared to microarray profiling.