5374527 High resolution DNA sequencing method using low viscosity medium

1995 ◽  
Vol 13 (4) ◽  
pp. 762
2002 ◽  
Vol 23 (10) ◽  
pp. 1441 ◽  
Author(s):  
Valessa Barbier ◽  
Brett A. Buchholz ◽  
Annelise E. Barron ◽  
Jean-Louis Viovy

1993 ◽  
Vol 144 ◽  
pp. 303-306 ◽  
Author(s):  
A. Manzin ◽  
S. Paolucci ◽  
P. Lampertico ◽  
S. Menzo ◽  
M.G. Rumi ◽  
...  

BMC Genomics ◽  
2014 ◽  
Vol 15 (1) ◽  
pp. 325 ◽  
Author(s):  
Yu Bai ◽  
Min Ni ◽  
Blerta Cooper ◽  
Yi Wei ◽  
Wen Fury

1996 ◽  
Vol 47 (1-2) ◽  
pp. 114
Author(s):  
Martina Bielefeld ◽  
Ella van den Berg-Loonen ◽  
Paul Savelkou ◽  
Lennart Björkesten

BioTechniques ◽  
1997 ◽  
Vol 22 (4) ◽  
pp. 653-656 ◽  
Author(s):  
Reiko Ohara ◽  
Ayako Tanaka ◽  
Osamu Ohara

2016 ◽  
Vol 78 (6) ◽  
pp. 516-522
Author(s):  
Joseph E. Conley ◽  
Alex J. Meisel ◽  
James J. Smith

This lesson is designed to facilitate student understanding of the molecular structure of DNA, the cellular processes involved in DNA replication, and how these principles were applied to develop a method to determine the nucleotide sequence of DNA. The lesson employs an active and cooperative learning approach accomplished via a modified jigsaw exercise. The specific replication/sequencing process in this lesson is Sanger's dideoxy method of DNA sequencing. In conjunction with related lessons in lecture and lab, students read the relevant section of an appropriate introductory biology textbook and/or view videos explaining how Sanger's dideoxy chain-termination sequencing method works. Students working in four teams (A, C, G, and T) then use green, blue, brown, and red M&M's as nucleotides to build a model of the process. Plain M&M's represent deoxynucleotide triphosphates (dNTPs), while peanut M&M's represent the “terminator” dideoxynucleotide triphosphates (ddNTPs). The lesson addresses Next Generation Science Standards and learning goals typically found in college biology courses at introductory and advanced levels.


1981 ◽  
Vol 1 (3) ◽  
pp. 243-252 ◽  
Author(s):  
G. F. Hong

A DNA sequencing method has been developed whereby DNA that has been cloned in a single-stranded bacteriophage vector can be sequenced from both ends. The method involves first making a minus-strand sense template from a single-stranded insert in the vector MJ3mp2 using a flanking primer, and then sequencing the synthesized template using the dideoxynucleotide termination method (Sanger et al., 1977, 1980) with a second primer. Special conditions are described under which the first primer is easily removed after making the templat% and sequencing in the opposite direction can be done in the normal way (Sanger et al., 1980) without separating the double strands. This method renders it possible to read up to twice the amount of sequence data from a long insert and also to check short inserts by producing complementary sequence patterns.


Sign in / Sign up

Export Citation Format

Share Document