Sequencing, Finishing, and Analysis in the Future Meeting

The 11th annual SFAF Meeting will be held June 1-3, 2016
La Fonda Hotel in Santa Fe, NM

The meeting will begin at 8:30 am on Wednesday, June 1st.
Download the 2016 Meeting Guide (pdf).


“Sequencing, Finishing and Analysis in the Future” (SFAF) is an annual meeting dedicated to bringing together experts in the genomics field—including representatives from the industries that serve this specialized scientific community.

The meeting focuses on laboratory methods and computational tools used to help sequence, assemble, and finish genomes, including new sequencing technologies, which promise high-throughput results by sequencing more base-pairs per run at longer read-lengths.

Keynote Speakers:

  • Mike Gilmore, Department of Ophthalmology, Harvard Medical School
  • Pavel Pevzner, Ronaly R. Taylor Professor of Computer Science and Director of the NIH Center for Computational Mass Spectrometry at UCSD
  • Joseph Petrosino, Department of Molecular Virology and Microbiology, Baylor College of Medicine

Download the 2016 SFAF meeting invitation (pdf).

Areas of emphasis

Genome Sequencing

  • Sequencing strategies and technology advancements using the various NGS platforms
  • De novo sequencing, re-sequencing, Human seq., RNA seq., metagenomics, etc.
  • Sequencing applications for metagenomics, transcriptomics, diagnostics, and biosurveillance

Genome Assembly

  • Whole genome assemblers and integration of next generation data
  • De novo assemblers for short reads, hybrid assemblers 
  • Single cell and metagenomic assemblies

Genome Improvement

  • Next generation finishing tools, technologies and pipelines
  • Human Genomics and genome improvement
  • Quality standards for new technologies and mixed data sets
  • Single cell / cell sorting and metagenomic finishing

Genome Analysis

  • Genome annotation and pathway identification tools and pipelines
  • Comparative genomics, re-sequencing, SNPs, structural variation
  • Large scale data management, cloud computing
  • Analysis for metagenomics, antimicrobial resistance, and forensics

Applications of NGS

  • Bringing sequence to the clinic (i.e., diagnostics)
  • Human, non-human, and infectious disease applications
  • Gene editing, synthetic genomics, forensics, and biosurveillance
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