A

Andrews, T. Daniel, Jeelall, Yogesh, Talaulikar, Dipti, Goodnow, Christopher C., and Field, Matthew A. (2016) DeepSNVMiner: a sequence analysis tool to detect emergent, rare mutations in subsets of cell populations. PeerJ, 4. e2074. pp. 1-13.

B

Brown, Peter, RELISH Consortium, and Zhou, Yaoqi (2019) Large expert-curated database for benchmarking document similarity detection in biomedical literature search. Database: the journal of biological databases and curation, 2019. baz085.

H

Harel, Roi, Alavi, Shauhin, Ashbury, Alison M., Aurisano, Jillian, Berger-Wolf, Tanya, Davis, Grace H., Hirsch, Ben T., Kalbitzer, Urs, Kays, Roland, Mclean, Kevin, Núñez, Chase L., Vining, Alexander, Walton, Zea, Havmøller, Rasmus Worsøe, and Crofoot, Margaret C. (2022) Life in 2.5D: Animal Movement in the Trees. Frontiers in Ecology and Evolution, 10. 801850.

S

Shafee, Thomas, and Cooke, Ira (2016) AlignStat: a web-tool and R package for statistical comparison of alternative multiple sequence alignments. BMC Bioinformatics, 17 (1). pp. 1-6.

V

van de Pol, M., Brouwer, L., and Cockburn, A. (2020) R package hiphop: parentage assignment using bi-allelic genetic markers. Statistical software. [Creative Work]

W

Waardenberg, Ashley J., and Field, Matthew A. (2019) consensusDE: an R package for assessing consensus of multiple RNA-seq algorithms with RUV correction. PeerJ, 7. e8206. pp. 1-16.