Sequencing of real-world samples using a microfabricated hybrid device having unconstrained straight separation channels

Electrophoresis. 2003 Nov;24(21):3762-8. doi: 10.1002/elps.200305616.

Abstract

We describe a microfabricated hybrid device that consists of a microfabricated chip containing multiple twin-T injectors attached to an array of capillaries that serve as the separation channels. A new fabrication process was employed to create two differently sized round channels in a chip. Twin-T injectors were formed by the smaller round channels that match the bore of the separation capillaries and separation capillaries were incorporated to the injectors through the larger round channels that match the outer diameter of the capillaries. This allows for a minimum dead volume and provides a robust chip/capillary interface. This hybrid design takes full advantage, such as sample stacking and purification and uniform signal intensity profile, of the unique chip injection scheme for DNA sequencing while employing long straight capillaries for the separations. In essence, the separation channel length is optimized for both speed and resolution since it is unconstrained by chip size. To demonstrate the reliability and practicality of this hybrid device, we sequenced over 1000 real-world samples from Human Chromosome 5 and Ciona intestinalis, prepared at Joint Genome Institute. We achieved average Phred20 read of 675 bases in about 70 min with a success rate of 91%. For the similar type of samples on MegaBACE 1000, the average Phred20 read is about 550-600 bases in 120 min separation time with a success rate of about 80-90%.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 5 / chemistry*
  • Ciona intestinalis
  • DNA / chemistry*
  • DNA / genetics
  • Electrophoresis, Capillary / instrumentation
  • Electrophoresis, Capillary / methods
  • Equipment Design
  • Humans
  • Miniaturization / instrumentation
  • Miniaturization / methods
  • Molecular Sequence Data
  • Oligonucleotide Array Sequence Analysis

Substances

  • DNA