AML43

<p>1242 SNAs from sequencing of leukemia patient at two timepoints. All SNAs
    are filtered to be from copy-number-neutral region.</p>

datasets

A statistical framework and computational procedure for identifying
the sub-populations within a tumor, determining the mutation profiles of each
subpopulation, and inferring the tumor's phylogenetic history. The input are
variant allele frequencies (VAFs) of somatic single nucleotide alterations
(SNAs) along with allele-specific coverage ratios between the tumor and matched
normal sample for somatic copy number alterations (CNAs). These quantities can
be directly taken from the output of existing software. Canopy provides a
general mathematical framework for pooling data across samples and sites to
infer the underlying parameters. For SNAs that fall within CNA regions, Canopy
infers their temporal ordering and resolves their phase.  When there are
multiple evolutionary configurations consistent with the data, Canopy outputs
all configurations along with their confidence assessment.

Yuchao Jiang

AML43: SNA input for primary tumor and relapse genome of leukemia patient from Ding et al. Nature 2012.

Description

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Examples