Selected Publications 

  • Gable D, Gaysinkaya V, Atik C, Talbot C, Kang B-H, Stanley S, Pugh E, Amat-Codina N, Schenk K, Arcasoy M, Brayton C, Florea L, and Armanios M (2019). The nuclear exosome targeting component ZCCHC8 is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation, Genes & Development, In press.
  • Lee CJ, Florea L, Sears CL, Maruthur N, Potter JJ, Schweitzer M, Magnuson T, and Clark JM (2019). Changes in gut microbiome after bariatric surgery versus medical weight loss in a pilot randomized trial, Obes Surg. doi: 10.1007/s11695-019-03976-4. [Medline]
  • Kelley DZ, Flam EL, Guo T, Danilova LV, Zamuner F, Bohrson C, Considine M, Windsor EJ, Bishop JA, Zhang C, Koch WM, Sidransky D, Westra WH, Chung CH, Califano JA, Wheelan S, Favorov AV, Florea L, Fertig EJ, and Gaykalova DA (2018). Functional characterization of alternatively spliced GSN in head and neck squamous cell carcinoma, Transl Res. pii: S1931-5244(18): 30108-7. [Medline]
  • ​Afsari B, Guo T, Considine M, Florea L, Kagohara LT, Stein-O'Brien GL, Kelley D, Flam E, Zambo K, Ha PK, Geman D, Ochs MF, Califano JA, Gaykalova DA, Favorov AV, and Fertig EJ (2018). Splice Expression Variation Analysis (SEVA) for inter-tumor heterogeneity of gene isoform usage in cancer, Bioinformatics 34(11):1859-1867. [Medline]
  • Yang G and Florea L (2017). JULiP: An efficient model for accurate intron selection from multiple RNA-seq samples, IEEEXplore - 6th IEEE International Conference on Computational Advances in Bio and Medical Sciences (ICCABS), 1-15. doi: 10.1109/ICCABS.2016.7802769 [Free text]
  • Parry EM, Gable DL, Stanley SE, Khalil SE, Antonescu V, Florea L, and Armanios M (2017). Germline mutations in DNA repair genes in lung adenocarcinoma, J. Thorac. Oncol. 12(11):1673-1678. [Medline]
  • Song L, Shankar D, and Florea L (2016). Rascaf: Improving genome assembly with RNA-seq data, The Plant Genome 9(3), doi: 10.3835/plantgenome2016.03.0027 [Full text]
  • Song L, Sabunciyan S, and Florea L (2016). CLASS2: Accurate and efficient splice variant annotation from RNA-seq reads, Nucl. Acids Res. 44(10):e98. [Medline]
  • Canzar S and Florea L (2016). Computational methods for transcript assembly from RNA-seq reads, In Computational Methods for Next Generation Sequencing Data Analysis 2016, Editors: Ion Mandoiu and Alexander Zelikovsky, Wiley-Interscience, John Wiley & Sons, Inc., Hoboken, NJ, 199-216.
  • Song L and Florea L (2015). Rcorrector: efficient and accurate error correction for Illumina RNA-seq reads, GigaScience4:48. [Full text]
  • Wang Z, Ceniccola K, Florea L, Wang BD, Lee NH, and Kumar A (2015). Viral non-coding RNA inhibits HNF4α expression in HCV associated hepatocellular carcinoma, Infectious Agents and Cancer 10(1):19. [Medline]
  • Song L, Florea L, and Langmead B (2014). Lighter: fast and memory-efficient error correction without counting, Genome Biology15:509. [Medline]
  • Bao W, Florea L, Wu N, Wang Z, Banaudha K, Qian J, Houzet L, Kumar R, and Kumar A (2014). Loss of nuclear PTEN in HCV-infected human hepatocytes, Infectious Agents and Cancer9:23. [Full text]
  • Florea L and Salzberg SL (2013). Genome-guided transcriptome assembly in the age of next generation sequencing, IEEE/ACM Trans. Computational Biology and Bioinformatics, 10(5):1234-40. [PubMed,Full text]
  • Florea L, Song L and Salzberg SL (2013). Thousands of exon skipping events differentiate splicing patterns in sixteen human tissues, F1000Research 2013, 2:188 (doi: 10.12688/f1000research.2-188.v1). [PubMed,Open access]
  • Eswaran J, Horvath A, Godbole S, Reddy SD, Mudvari P, Ohshiro K, Cyanam D, Nair S, Fuqua SAW, Polyak K, Florea LD, and Kumar R (2013). RNA sequencing of cancer reveals novel splicing alterations, Sci. Rep. 3:1689. [Medline]

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