+** Genomics and Epigenomics
++ *NGS* and array-based Genomics and Epigenomics of complex human
+ diseases using *RNA-seq*, targeted DNA sequencing, *RRBS*, Illumina
+ bead arrays, and Affymetrix microarrays from sample collection to
+ publication.
++ Reproducible, scalable bioinformatics analysis using make,
+ *nextflow*, and *cwl* based workflows on cloud- and cluster-based
+ systems on terabyte-scale datasets
++ Alignment, annotation, and variant calling using existing and
+ custom-written software, including *GATK*, *bwa*, *STAR*, and
+ *kallisto*.
++ Correcting for and experimental design to overcome multiple
+ testing, confounders, and batch effects using Bayesian and
+ frequentist methods approaches
+# + Using evolutionary genomics to identify causal human variants