Skip to main content

Introduction to Bioinformatics


           Bioinformatics is branch of biological and biomedical sciences and it is an application for the management of the vast biological information. Technically, Bioinformatics is the combination of biological sciences and information technology. In this field, the computers, softwares and online databases are used to gather, store, analyze and integrate biological information and genetic information. These information can then be applied to gene-based drug discovery, protein engineering and development. With the help of this, an investigator can store or analyze the genetic information in understanding the human diseases  and in the identification of new potential molecular targets and drug discovery. Bioinformatics can also be applied to study the fundamental biomedical problems. 

Biological Databases:

Huge amount of data of nucleotides, proteins and structures can not be written in a book.. Its gonna take a lot of time and effort to write those data.. But, technology has evolved in a such a way that we can practically store vast amount of data in an online databases and these databases are publically available. 


Data generated are deposited in online databases which are publically accessible. These data include nucleotide sequences of genes or amino acid sequences of proteins. and there are some databases which have the data of function, structure, localization, mutations, and also the similarities of biological sequences from species to species. (Localization includes both chromosomal and cellular). 

There are mainly three types of databases: 

1) Nucleotide Sequence Database
2) Protein Sequence Database
3) Molecular Structure Database. 

Examples of Databases: 

EMBL = European Molecular Biology Laboratory. 

GenBank = This is nucleotide database and it is maintained by NCBI (National Center for Biotechnology Information). 

NCBI is itself a database which has contains lot of biological information and it is a part of NIH. 

DDBJ = DNA Data Bank of Japan. 

Unigen = Non-redundant database of gene-oriented clusters. 

EBI Genomes = Complete Genome Statistics. 

Ensembl = Software to produce and maintain automatic annotations of eukaryotic genomes. 

SWISS-PROT = Manually Curated biological database of protein sequences. 

PIR = Protein Information Resource, to support genomic and proteomic research. 

UniProt = Universal Protein Database, a central repository of protein data. 

PROSITEIt =  Protein Families and Domains Database. 

Pfam = Protein families database of alignments and Hidden Markov Models. 

PDB = Protein Data Bank, 3-D structural data of proteins and nucleic acids. 

SCOP = Structural Classification of Proteins, it classifies the protein 3-D structures in hierarchy. 

CATH = Class Architecture Topology Homologous Super Family, hierarchical classification of protein domain structures. 

KEGG = Kyoto Encyclopedia of Gene and Genomes, collection of online databases of genomes, biological chemicals and enzymatic pathways. 

Comments

Popular posts from this blog

Statistics in Flow Cytometry Data and "MFI" values

                                 The speed of the flow cytometry offers wide range of data points and data plots. Due to its sensitivity and versatility, it has been used extensively. Flow cytometer can detect up to 1000s of cells per second.. But, it should be noted that the flow cytometry also involves the statistics, its significance, calculating the fluorescence intensity..                Statistics in flow cytometry involves, total number of data points acquired, percentage population, most importantly mean and median fluorescence intensity, and others. Most of us get confused about the term "MFI", whether it means mean fluorescence intensity or median fluorescence intensity.. Truth is, both.. It means it can be described as either mean or median fluorescence intensity. Some researchers use Mean for MFI and some use Median for MFI values.  (Keeping in mind that, consideration of statistics in flow cyomtery also depends on the type of Application you are interest

Protocol: Chromosomal DNA Isolation from Bacteria

1.       Spin down 50-100 ml well-grown bacteria, 3600 rpm,15min. 2.     Resuspend bacteria with 20 ml Buffer S, immediately add 100 µl ProteinaseK (10 mg/ml). Vortex to make sure no chunks. 3.       Add 2 ml of 20% SDS, mix gently by inverting. 4.       Incubate the mixture at 65 o C for 1 hr with inverting every 15 min. 5.     Add 10 ml of phenol and 10 ml of chloroform, mix thoroughly by inverting for 5 min, spin at 3600 rpm for 20 min. 6.       Transfer supernatant to a new tube, add 0.6 volume of isopropanol. Mix gently by inverting. You will see cotton-like genomic DNA. 7.       Hook out the cotton-like DNA to a 1.5 ml tube; wash with cold 70% ethanol. 8.      Dry DNA at RT, dissolve DNA in 500 µl H 2 O (50 o C or 4 o C overnight). 9.      Add 5 µl DNase-free RNase A (20 mg/ml stock) to the DNA. Incubate at 37 o C for 30 min. 10.   Add 500 µl phenol, mix, spin at 3600 rpm for 20 min. Repeat phenol extraction once if necessary. 11.   Tr

Gene Cloning Technique

Gene Cloning Technique in Molecular Biology Field Involves the following steps: 1.a) Isolation of Genetic Material and Gene Sequence of Interest.  First, cells are lysed using detergent or lysozyme enzymes which disrupts the plasma membrane and release the genetic material along with the macro molecules such proteins and RNA molecules. Cell contents are then treated with protease to disrupt the proteins and RNase to destroy the RNA. Cell debris are then pelleted using centrifuge and supernatant containing DNA is transferred to a fresh and clean tube. A proper amount of Ethanol is added to this supernatant and precipitated using centrifuge. Supernatant is discarded and the pellet which has DNA is suspended using a proper suitable buffer.  Primers are designed for the specific gene sequence of interest which will be used for the cloning procedure.  Gene sequence is then amplified using PCR (Polymerase Chain Reaction) which will yield in many copies of the gene sequence.