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.
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Massively parallel RNA sequencing, commonly known as RNA-seq, provides a more detailed picture of transcriptomes compared to microarray profiling.