If you made any changes in Pure, your changes will be visible here soon.

Personal profile

Research interests

The development of genomics, bioinformatics and statistical methods as they apply to the study of cancer biology and medicine. A particular focus on the translation of genomics data from whole genome, exome and transcriptome sequencing into clinically actionable observations and personalized cancer therapies.

Fingerprint Dive into the research topics where Malachi Griffith is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 10 Similar Profiles
Genome Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Mutation Medicine & Life Sciences
RNA Sequence Analysis Medicine & Life Sciences
Transcriptome Medicine & Life Sciences
Genes Medicine & Life Sciences
Breast Neoplasms Medicine & Life Sciences
High-Throughput Nucleotide Sequencing Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2003 2019

2 Citations (Scopus)

Accounting for proximal variants improves neoantigen prediction

Hundal, J., Kiwala, S., Feng, Y. Y., Liu, C. J., Govindan, R., Chapman, W., Uppaluri, R., Swamidass, J., Griffith, O., Mardis, E. R. & Griffith, M., Jan 1 2019, In : Nature Genetics. 51, 1, p. 175-179 5 p.

Research output: Contribution to journalArticle

Major Histocompatibility Complex
1 Citation (Scopus)

A Spontaneous Aggressive ERα+ Mammary Tumor Model Is Driven by Kras Activation

Campbell, K. M., O'Leary, K. A., Rugowski, D. E., Mulligan, W. A., Barnell, E. K., Skidmore, Z. L., Krysiak, K., Griffith, M., Schuler, L. A. & Griffith, O., Aug 6 2019, In : Cell Reports. 28, 6, p. 1526-1537.e4

Research output: Contribution to journalArticle

Open Access
Chemical activation
Breast Neoplasms

Best practices for bioinformatic characterization of neoantigens for clinical utility

Richters, M. M., Xia, H., Campbell, K. M., Gillanders, W., Griffith, O. & Griffith, M., Aug 28 2019, In : Genome medicine. 11, 1, 56.

Research output: Contribution to journalReview article

Open Access
Computational Biology
Practice Guidelines

Noninvasive Detection of High-Risk Adenomas Using Stool-Derived Eukaryotic RNA Sequences as Biomarkers

Geneoscopy Scientists, Sep 1 2019, In : Gastroenterology. 157, 3, p. 884-887.e3

Research output: Contribution to journalArticle

Open Access
Early Detection of Cancer
4 Citations (Scopus)

Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples

Barnell, E. K., Ronning, P., Campbell, K. M., Krysiak, K., Ainscough, B. J., Sheta, L. M., Pema, S. P., Schmidt, A. D., Richters, M., Cotto, K. C., Danos, A. M., Ramirez, C., Skidmore, Z. L., Spies, N. C., Hundal, J., Sediqzad, M. S., Kunisaki, J., Gomez, F., Trani, L., Matlock, M. & 4 others, Wagner, A. H., Swamidass, J., Griffith, M. & Griffith, O., Apr 1 2019, In : Genetics in Medicine. 21, 4, p. 972-981 10 p.

Research output: Contribution to journalArticle

Open Access