Name: Sample Student
ORCID: 0000-0000-0000-0000
Position Title: Master's Student / Research Assistant
Email: sample.student@university.edu

Education/Training

Institution and Location Degree (if applicable) Start Date
MM/YYYY
Completion Date
MM/YYYY
Field of Study
Harvard University
Boston, MA
MS 08/2013 05/2015 (Expected) Bioinformatics and Integrative Genomics
Johns Hopkins University
Baltimore, MD
BS 08/2009 05/2013 Biomedical Engineering, Applied Mathematics and Statistics

A. Personal Statement

My longterm research interests involve [research interests]. I am currently a research assistant, focusing on [research area]. My background includes experience in [specific techniques/methods]. I have developed expertise in [key skills/methods relevant to future work]. My recent work on [describe recent projects] has prepared me to [what do you hope to do with these skills]. During my PhD, I aim to [goals for PhD training and beyond].

B. Positions, Scientific Appointments, and Honors

Positions and Scientific Appointments

2013 – Present: Graduate Research Assistant, mentored by Dr. Mentor One in collaboration with Dr. Mentor Two, Harvard Medical School
2014 – Present: Co-chair for the Graduate Women in Science and Engineering Student Group, Harvard University
06/2012 – 08/2012: Summer research intern in the BIG Summer Program, mentored by Dr. Summer, Harvard Medical School
08/2011 – 12/2011: Teaching Assistant for Intro to Optimization, mentored by Dr. Teacher, Johns Hopkins University

Honors

2013: National Science Foundation Graduate Research Fellowship Program awardee
2009 – 2013: Johns Hopkins University Dean’s list
2009: Intel Science Talent Search Semi Finalist

C. Contributions to Science

1. A more complete understanding of chronic lymphocytic leukemia:

Advancements in high-throughput sequencing technologies have uncovered tremendous genetic, epigenetic, and transcriptional heterogeneity in chronic lymphocytic leukemia (CLL) but its impact on clinical course is not well understood. I have established a close collaboration with the Wu lab at the Dana-Farber Cancer Institute, where I have focused on developing and applying bioinformatics methods for assessing variability of single cell gene expression, calling mutations from single cell qt-qPCR data, differential expression and gene set enrichment tests for both bulk and single cell, RNA-sequencing and targeted qt-qPCR data. Our collaboration has led to many scientific findings that contribute to a more complete understanding of CLL.

Publications:
  • Landau DA, Clement K, Ziller MJ, Boyle P, Fan J, Gu H, Stevenson K, Sougnez C, Wang L, Li S, Kotliar D, Zhang W, Ghandi M, Garraway L, Fernandes SM, Livak KJ, Gabriel S, Gnirke A, Lander ES, Brown JR, Neuberg D, Kharchenko PV, Hacohen N, Getz G, Meissner A, and Wu CJ. Locally disordered methylation forms the basis of intratumor methylome variation in chronic lymphocytic leukemia. Cancer Cell 2014, Dec 8; 26(6):813-25
  • Burger, JA, Landau DA, Taylor-Weiner A, Zhang H, Sarosiek K, Wang L, Stewart C, Fan J, Hoellenriegel H, Sivina M, Dubuc AM, Fraser C, Han Y, Livak K, Zou L, Wan Y, Konoplev SN, Sougnez C, Abruzzo LV, Carter CL, Keating MJ, Davids M, Wierda WG, Cibulskis K, Zenz T, Werner K, Kharchencko P, Cin PD, Neuberg D, Kantarjian H, Lander E, Gabriel S, O'Brien S, Letai A, Weitz D, Nowak MA, Getz G, and Wu CJ. Clonal evolution in patients with chronic lymphocytic leukemia developing resistance to BTK inhibition. Cancer Discovery (in press)
  • Pleiotropic effects of splice variants generated by SF3B1 mutations in chronic lymphocytic leukemia (in preparation)

2. Statistical methods and software for analyses of single cell data:

While heterogeneity within cellular systems has long been widely recognized, only recently have technological advances enabled measurements to be made on a single cell level. Applying traditional bulk analysis methods on single cells has met with varied degrees of success due to the high levels of technical as well as biological stochasticity and noise inherent in single cell measurements. Therefore, novel statistical methods are needed to identify and characterize heterogeneity in single cells. In the Kharchenko lab, I have focused on developing methods for analyzing single cell data, including differential expression analysis methods that takes into account sources of technical noise inherent to single cell RNA-seq data, clustering methods to identify pathways and gene sets that exhibit coordinated variability, and methods for spatial placement of cell subpopulations based on expression signatures. This work has led to the development of various statistical methods available as software for the scientific community.

Publications/Presentations:
  • Fan J, Salathia N, Liu R, Kaeser G, Yung Y, Herman J, Kaper F, Fan JB, Zhang K, Chun J, and Kharchenko PV. Characterizing transcriptional heterogeneity through pathway and gene set overdispersion analysis (manuscript in revision)
  • Fan J, Salathia N, Liu R, Kaeser G, Yung Y, Herman J, Kaper F, Fan JB, Zhang K, Chun J, and Kharchenko PV. Characterizing transcriptional heterogeneity through pathway and gene set overdispersion analysis. American Society of Human Genetics, 2014 (poster presentation)

3. Improving the representation of women in STEM:

Women are underrepresented in science, technology, engineering, and math (STEM) fields. Improving the representation of women in STEM is pertinent to workplace diversity, gender equality, and American innovation. To help address this issue, I have been involved in a number of outreach efforts. I was the lead software engineer for the BioHazardz 3D video games, which teach students the fundamentals of protein evolution through an intuitive and attractive gaming environment. I founded the 501(c)3 non-profit CuSTEMized and developed the website, software, graphics, and content to enable parents to generate and download free personalized motivational ebooks to help girls envision themselves in science, technology, engineering, and math. I am the co-chair of the Harvard Graduate Women in Science and Engineering student group. I manage and lead organization of networking, professional development, and mentoring events for women in natural sciences, social sciences, and engineering at Harvard University.

D. Scholastic Performance

Johns Hopkins University

Year Course Title Grade
2009 Honors Multivariable Calculus A
2010 Data Structures B+
2011 Statistical Mechanics/Thermo A-

Harvard University

Year Course Title Grade
2013 Statistical Inference B+
2014 Selected Topics in High Dimensional Analysis SAT
2015 (Additional Relevant Coursework) AU
SAT: Verbal 750/800, Math 780/800, Writing 720/800
GRE: Verbal 165/170, Quantitative 170/170, Analytical Writing 5.0/6.0
MCAT: Total 520 ( 131/130/130/129)
TOEFL: Total 115 ( Reading: 29, Listening: 30, Speaking: 28, Writing: 28)