2-Color encoding solid phase minisequencing. 2011

Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
State Key Laboratory of Bioelectronics, Southeast University, Nanjing, 210096, China.

Solid phase minisequencing is an effective single nucleotide determination technique. However, two main methods currently used are both time and money consuming. Here, we introduced a more economical and time efficient approach, called 2-color encoding minisequencing, in which four varieties of nucleotides were labeled by the combination of two fluorescence dyes. Such code was sensitive for different nucleotides, and the sequencing results were highly uniform and repeatable.

UI MeSH Term Description Entries
D008969 Molecular Sequence Data Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories. Sequence Data, Molecular,Molecular Sequencing Data,Data, Molecular Sequence,Data, Molecular Sequencing,Sequencing Data, Molecular
D003124 Colorimetry Any technique by which an unknown color is evaluated in terms of standard colors. The technique may be visual, photoelectric, or indirect by means of spectrophotometry. It is used in chemistry and physics. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
D004247 DNA A deoxyribonucleotide polymer that is the primary genetic material of all cells. Eukaryotic and prokaryotic organisms normally contain DNA in a double-stranded state, yet several important biological processes transiently involve single-stranded regions. DNA, which consists of a polysugar-phosphate backbone possessing projections of purines (adenine and guanine) and pyrimidines (thymine and cytosine), forms a double helix that is held together by hydrogen bonds between these purines and pyrimidines (adenine to thymine and guanine to cytosine). DNA, Double-Stranded,Deoxyribonucleic Acid,ds-DNA,DNA, Double Stranded,Double-Stranded DNA,ds DNA
D001483 Base Sequence The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence. DNA Sequence,Nucleotide Sequence,RNA Sequence,DNA Sequences,Base Sequences,Nucleotide Sequences,RNA Sequences,Sequence, Base,Sequence, DNA,Sequence, Nucleotide,Sequence, RNA,Sequences, Base,Sequences, DNA,Sequences, Nucleotide,Sequences, RNA
D017404 In Situ Hybridization, Fluorescence A type of IN SITU HYBRIDIZATION in which target sequences are stained with fluorescent dye so their location and size can be determined using fluorescence microscopy. This staining is sufficiently distinct that the hybridization signal can be seen both in metaphase spreads and in interphase nuclei. FISH Technique,Fluorescent in Situ Hybridization,Hybridization in Situ, Fluorescence,FISH Technic,Hybridization in Situ, Fluorescent,In Situ Hybridization, Fluorescent,FISH Technics,FISH Techniques,Technic, FISH,Technics, FISH,Technique, FISH,Techniques, FISH
D017422 Sequence Analysis, DNA A multistage process that includes cloning, physical mapping, subcloning, determination of the DNA SEQUENCE, and information analysis. DNA Sequence Analysis,Sequence Determination, DNA,Analysis, DNA Sequence,DNA Sequence Determination,DNA Sequence Determinations,DNA Sequencing,Determination, DNA Sequence,Determinations, DNA Sequence,Sequence Determinations, DNA,Analyses, DNA Sequence,DNA Sequence Analyses,Sequence Analyses, DNA,Sequencing, DNA
D036641 Microscopy, Fluorescence, Multiphoton Fluorescence microscopy utilizing multiple low-energy photons to produce the excitation event of the fluorophore (endogenous fluorescent molecules in living tissues or FLUORESCENT DYES). Multiphoton microscopes have a simplified optical path in the emission side due to the lack of an emission pinhole, which is necessary with normal confocal microscopes. Ultimately this allows spatial isolation of the excitation event, enabling deeper imaging into optically thick tissue, while restricting photobleaching and phototoxicity to the area being imaged. Fluorescence Microscopy, Multiphoton,Multiphoton Fluorescence Microscopy,Multiphoton Excitation Microscopy,Excitation Microscopies, Multiphoton,Excitation Microscopy, Multiphoton,Microscopies, Multiphoton Excitation,Microscopy, Multiphoton Excitation,Microscopy, Multiphoton Fluorescence,Multiphoton Excitation Microscopies

Related Publications

Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
January 1997, Human genetics,
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
January 2002, Methods in molecular biology (Clifton, N.J.),
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
January 2003, Methods in molecular biology (Clifton, N.J.),
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
January 1993, EXS,
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
January 1996, Methods in molecular biology (Clifton, N.J.),
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
January 1998, Methods in molecular biology (Clifton, N.J.),
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
November 2001, Genome research,
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
January 1992, Clinical chemistry,
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
January 1998, Methods in molecular biology (Clifton, N.J.),
Jing Tu, and Yunfei Bai, and Qinyu Ge, and Qi Yang, and Zuhong Lu
September 1996, Clinical chemistry,
Copied contents to your clipboard!