Illumina HiSeq 2500
  In Rapid Mode generates 125-150Gb of sequence data (2x250) per lane of a 2 lane flow cell, or runs a single flow cell (8 lane flow cell) in “High Output Run Mode” and generates 62.5 Gb of sequence data (2x125) per lane. This machine can operate with twice this capacity in either Rapid Mode (2x2 lanes) or high output mode (2x8 lane). In high output mode it generates some 2 billion reads per flow cell.

PacBio Sequel
   We are also running a Sequel instrument. Because the SMRT approach involves sequencing large, intact DNA segments, it dramatically improves or enables several genomics approaches, including: (1) de novo genome assembly, (2) detecting structural variants, (3) constructing full haplotypes, (4) more accurate transcriptome assembly, (5) detecting epigenetic modifications, and (6) direct RNA sequencing to measure post-transcriptional modifications and secondary RNA structure that is lost during cDNA synthesis. Each SMRTcell generates approximately 4Gb of DNA sequence data. Read lengths are currently limited to about 20-30,000 bases. The Sequel is undergoing rapid improvements and the read length will likely increase in the near future.

Applied Biosystems 3730xl DNA Analyzer
    In its current configuration, the ABI 3730xl will generate 1,152 (12 x 96) sample reads a day, with each read containing a QV20 read length of approximately 900 bases. This machine can be configured to produce twice as many sample reads a day. For the faster configuration read lengths are shorter with an average QV20 of 650 bases. A second machine is setup for running fragment analysis with either Liz or Rox standards.

Geneious Software
    BYU users can send a request to the College of Life Sciences Computer Support group and ask that they install Geneious on your computer. This is one option if you are looking for software in which to open the DNA sequencing trace files that you download from our server. There are other software options available (please see below for a link to BioEdit a PC compatible program that is free).

Bioinformatics and Intensive Computation 
    For the computational aspects of any project, please use the resources of the BYU Fulton Supercomputing Lab, which is already set up with a full suite of bioinformatics and phylogenetic analysis software.  The Fulton Supercomputing Lab offers a total of 16,928 CPU cores and about 50 TB of memory across 943 compute nodes. It is supported by approximately 2 petabytes of storage.  All nodes have Red Hat Enterprise Linux 6.6. More detail is available at <https://marylou.byu.edu/documentation/resources>.

Other Equipment
   We have the equipment necessary to prepare and analyze DNA, RNA and the libraries made to run on the equipment we carry. Specifically we have a Fragment Analyzer by Advanced Analytical, an Agilent 2100 Bioanalyzer, a Megaruptor by Diagenode, a Hydroshear, a BluePippin for targeted size selection from Sage Science, a Caliper Gel Chip from PerkinElmer, a Qubit v3.0 Fluorometer, a Coulter Particle Counter, a Tissuelyser, a Turner Biosystems TBS-380 flourometer, and many other small equipment items needed for DNA handling and library preparation.

BYU Library has also created a resource page of

• Bioinformatics Subject Guide
• Molecular Biology Web Tools

Sequence Databases

• Genbank Home Page(NCBI)
• Genbank Blast Search
• European Bioinformatics Institute (EBI)
• Japanese GenomeNet
• Swiss Institute of Bioinformatics
• BIOSCI/bionet Electronic Newsgroup Network for Biology
• EMBnet

Other DNA Sequencing Facilities

• MSU Research Technology Support Facility
• University of Virginia Health Science Center Sequencing Facility
• Iowa State DNA Facility
• John Hopkins Synthesis & Sequencing Facility
• University of Missouri DNA Core Facility
• University of Utah Health Sciences High Throughput Genomics Facility

Tools

Sequence Tools on the Web:
Click on the links below in order to access the Sequencing Tools.

The Sequence Manipulation Suite - A collection of 30 different utilities for analyzing and manipulation sequence data.As seen in BioTechniques 28(6): 1102-1104.

A fairly complete list of proteomics tools maintained by ExPASy (Swiss Institute of Bioinformatics).

Database Searching and File Manipulation
EMBL Tools - Database Searching, Browsing and Analysis Tools.
BLAST to FASTA Format - Will convert NCBI BLAST output to FASTA Format.

DNA Tools
WebCutter - will produce a restriction map of a sequence you input.
Open Reading Frame Finder - identifies all open reading frames using the standard or alternative codes.
Biological Online Collaboration - multiple users can work together online on biological tasks.
Sanger Institute Software Solutions - many tools for manipulating DNA sequence.

Sequence Alignment
ESPript 3 - Tool to print a multiple alignment.
Multiple Sequence Alignment - At EBI.
Blast - align two sequences using BLAST
LALIGN - find multiple matching subsegments in two sequences

RNA Tools
mfold - RNA Secondary Structure Prediction.
RNAfold - Predict RNA secondary structure from sequence

Primers & Primer Design
Primer 3 - Picks PCR primers from nucleotide sequences you supply.
OligoCalc - Will calculate the T_M of your oligonucleotides.
Primer Analysis Software - NetPrimer and Beacon Designer free link.

Protein Tools
DNA to Protein Translator - Converts DNA sequences to protein sequences.
Peptide Property Calculator - Calculates Molecular Weight, Length of the Peptide, and Others.
Protein Calculator - Will calculate Molecular Weight, Charge, UV Absorbtion, Atom and Residue Counts, and Solvent Content.
PredictProtein - Prediction of transmembrane helix location and topology (Columbia University).

Miscellaneous
Centrifuge Helper - Helps to calculate g-values for various centrifuge models and rotors.

FreeWare Sequence Editing Software: (Download and install on your machine). Note: Please DO NOT install these software packages on DNASC computers, use Sequencher instead.
Chromas 2.4.3 A minimal cost software for handling trace files.
BioEdit - Biological Sequence Alignment Editor. (Freeware)

Sequence Analysis Software:
ClustalW2 - Multiple Sequence Alignment Program.
PHYLIP v3.57 - by Joe Felsenstein.
PAUP* v4.0 - by David Swofford.
TFPGA - Tools for Population Genetic Analyses, by Mark Miller.