Fluorescent dye-primer cycle sequencing using unpurified PCR products as templates; development of a protocol amenable to high-throughput DNA sequencing

This publication has 10 references indexed in Scilit:

• Direct DNA sequencing of PCR-amplified vector inserts following enzymatic degradation of primer and dNTPs.
  1994
• Improved fluorescent cycle sequencing protocol allows reading nearly 1000 bases.
  1994
• Variations on cycle sequencing.
  1994
• PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates.
  Proceedings of the National Academy of Sciences, 1994
• Direct sequencing of PCR products in agarose ge l slices
  Nucleic Acids Research, 1994
• High-throughput detergent extraction of M13 subclones for fluorescent DNA sequencing
  Nucleic Acids Research, 1994
• High-throughput purification of M13 templates for DNA sequencing.
  1993
• Direct sequencing of double-stranded PCR products without intermediate fragment purification; digestion with mung bean nuclease
  Nucleic Acids Research, 1993
• Large-scale production of DNA sequencing templates by microtitre format PCR
  Nucleic Acids Research, 1993
• Magnetic bead purification of M13 DNA sequencing templates
  Analytical Biochemistry, 1992