correlogram method for comparing bio-sequences - gandhali samant, m.s. computer science committee...
Post on 05-Jan-2016
240 Views
Preview:
TRANSCRIPT
Correlogram Method for comparing Bio-Sequences
- Gandhali Samant , M.S. Computer Science
Committee Dr. Debasis Mitra, PhD Dr. William Shoaff, PhD Dr. Alan Leonard, PhD
What is Sequence Comparison
Sequence Comparison – One of the most important primitive operations in computational biology.
Finding resemblance or similarity between sequences
Basis for many other more complex manipulations.
Used for database search, phylogeny development, clustering etc.
What is Sequence Comparison …Contd.
Two important notions are -Similarity – How similar are the two sequences? This gives a numeric score of similarity between two sequences
A G T C T CA T T G T C
--------------------------1 -1 1 -1 1 1 = 2
Alignment – Way of placing one sequence above other to make clear the correspondence between them.
A G T C G T CA _ T C _ T C
--------------------------1 -2 1 1 -2 1 1 = 1
What is Sequence Comparison …Contd.
Many methods have been proposed for sequence comparison.
Some Important ones include –Dynamic programming algorithms for sequence alignment - Global, Local or Semi-Global Alignment
Heuristic and Database Search Algorithms - BLAST,
FASTA.
What is Sequence Comparison …Contd.
Multiple sequence alignment AlgorithmsMultiple sequence alignment methods are mainly used when there is a need to extract information from a group of sequences.
Examples of situations in which these techniques are used include the determination of secondary or tertiary structures, characterization of protein families, identification of similar regions etc.
What is Sequence Comparison …Contd.
Also many miscellaneous techniques have been proposed for sequence comparison
Contact based sequence alignment
Using Correlation Images
Some methods have been proposed without using the fundamental tool of Sequence Alignment
Shortest unique substring
Background Study
Basic Concepts of Molecular Biology
BLAST
Clustering
Phylogeny Trees / Phylip
Basic Concepts of Molecular Biology
Proteins –Most substances in our body are proteins
Some of these are structural proteins and some are enzymes.
Proteins are responsible for what an organism is and what it does in physical sense.
Amino Acids –A protein is a chain of simple molecules called Amino Acids. There are total 20 amino acids
Basic Concepts of Molecular Biology
Nucleic Acids –Nucleic Acids encode information necessary to produce proteins They are responsible for passing recipe to subsequent generations. 2 types of nucleic acids present in living organisms,
RNA (ribonucleic acid) DNA (deoxyribonucleic acid).
BLAST
BLAST (Basic Local Alignment Search Tool)
BLAST algorithms are heuristic search methods
This method seeks words of length W (default=3 in blastP) that score at least T when aligned with the query and scored with the substitution matrix (e.g. PAM)
Clustering
Clustering It can be defined as “The process of organizing objects into groups whose members are similar in some way”
Phylogeny Trees / Phylip
Phylogeny -The context of evolutionary biology
Phylogeny TreesRelationships between different species and their common ancestors shown by constructing a tree.
PHYLIP, the Phylogeny Inference Package, is a package of programs for inferring phylogenies (evolutionary trees) from University of Washington .
What Phylip can do??
Data used by phylip.
Phylip…Contd.
Following are the programs used from Phylip package in this research.
FITCH - Estimates phylogenies from distance matrix data.
KITCH - Estimates phylogenies from distance matrix data.
NEIGHBOR - Produces an un-rooted tree
DRAWGRAM - Plots rooted phylogenies, cladograms, circular trees and phenograms in a wide variety of user-controllable formats. The program is interactive.
DRAWTREE - Similar to DRAWGRAM but plots unrooted phylogenies.
Our Approach …Correlogram
What is a Correlogram??
Representation of sequence in mathematical space.
3-D matrix of which 2 dimensions are the set of entities (e.g.. Amino Acids, Nucleic Acids) and third dimension is distance.
A T G C
D
3210
C
AT
G
Correlogram for Image Comparison
Correlogram method has already been used for Image comparison.“Image indexing using color correlograms” By Jing Huang,S Ravi Kumar, Mandar Mitra, Wei-Jing Zhu, Ramin Zabih
A color correlogram expresses how the spatial correlation of pairs of colors changes with the distance
Color correlogram has also been used recently for object tracking
Correlogram Usage in the field of Bioinformatics
Correlograms were used to analyze autocorrelation characteristics of active polypeptides.
MF Macchiato, V Cuomo and A Tramontano (1985), “Determination of the autocorrelation orders of proteins”
For analyzing spatial patterns in various experiments.– Giorgio Bertorelle and Guido Barbujanit (1995), “Analysis
of DNA Diversity by Spatial Auto Correlation”
In studies regarding patterns of transitional mutation biases within and among mammalian genomes
– Michael S. Rosenberg, Sankar Subramanian, and Sudhir Kumar (2003), “Patterns of Transitional Mutation Biases Within and Among Mammalian Genomes”
Constructing a Correlogram plane
Example Sequence ….. agcttactgt
If we calculate the appearance of every pair of
characters at distance 1 ..
The Correlogram Plane for distance 1 will be ->
Correlogram can be constructed as a set of frequencies for different distances.
A T G C
A 1 1
T 1 1 1
G 1 1
C 2
d = 1
Constructing a Correlogram plane…Contd.
Example Sequence ….. agcttactgt
Correlogram plane for d=0
A T G C
A 2
T 4
G 2
C 2
d = 0
Constructing a Correlogram plane…Contd.
Example Sequence ….. agcttactgt
Correlogram plane for d=2
A T G C
A 1 1
T 1 1 1
G 1
C 1 1
d = 2
Graphical Representation of Correlogram
Correlogram plane shown here is of a protein sequence for distance 0.
At distance 0 each character is compared with itself so we can see all the peaks at diagonal.
This is a Histogram.
0
0.05
0.1
A C D E F G H I K L M N P Q R S T V W YACDEFGHIKLM
NPQRSTVWY
Graphical Representation …Contd.
Similarly Correlogram frequencies for distance 1 and distance 2 can be represented as…
Normalization of Correlogram
Need for normalization – Finding similarity between sequences of different length.
For every correlogram plane, each value is divided by the total volume of that plane.
Extension - Gapped Correlogram
Gapped Correlogram - Consideration the gapped alignment of sequences
The reason is if a pair of character is at distance d, there is probability that in other sequence it might appear at distance d-1 or d+1.
Adding a ‘delta’ to Correlogram.
1
0.5 0.5
0.25 0.25
d -> 2 3 4 5 6
For every pair at distance n, frequency f and with delta = d, a fraction of frequency f/(2|n-distance|) is added at distances n-1,n-2… n-d and distances n+1,n+2… n+d.
Extension - Gapped Correlogram…Contd.
+ A T G C
A 1
0.5
T 0.5 0.5
0.5
G 0.5 0.5
C 1
A T G C
A 2 1
T 1 1
1
G 1 1
C 2
+ A T G C
A 1 0.5
T 0.5 0.5
0.5
G 0.5 0.5
C 1
D=3
D=4
D=2
Adding values to previous plane
Adding values to next plane
Delta = 1
Correlogram for Sequence Comparison
We are using these Correlograms for comparison of 2 sequences.
Correlograms were constructed using same set of distances for both the sequences being compared.
Then distance between each cell of two Correlograms (i.e. Two 3-D Matrices) is calculated as
dijk = (Sijk – S’ijk )2 / (1+ Sijk + S’ijk )where i, j and k are 3 dimensions.
These distances were then added to get a final distance between two sequences.
d = √ ∑ dijk
One major difference !!
Synthetic Data Experiments using Correlogram
Purpose To discriminate and compare the capability of correlogram-method with one of the "traditional" comparison techniques i.e. Smith-Waterman Dynamic Programming algorithms.
The reason for using DP algorithms for comparison was that they are the most standard method for sequence comparison.
The sequences used in these experiments were amino acid sequences
Synthetic Data Experiments…Contd.
In all the experiments, the pair of sequences was compared using both Correlogram method and DP Method.
Synthetic Data Experiments…Contd.
The experiments were designed as followsComparing a base sequence with its reverse sequenceWrap around the target sequence at different character length and measure the difference with respect to the reference sequence each time Delete an amino acid from target sequence and measure the difference with respect to the reference sequence each time Replace an amino acid at different location and measure the difference with respect to the reference sequence each time Add an amino acid from target sequence and measure the difference with respect to the reference sequence each time
Synthetic Data Experiments…Contd.
Comparing a base sequence with its reverse sequence.
-2
-1
0
1
2
3
4
5
1 2 3 4Iterations
Sco
res
Correlogram Score DP Score
Synthetic Data Experiments…Contd.
Wrap around the target sequence at different character length and measure the difference with respect to the reference sequence each time.
-1
0
1
2
3
4
5
0 2 4 6 8 10 12Iterations
Sco
re
Correlogram Score DP Score
Synthetic Data Experiments…Contd.
Delete an amino acid from target sequence and measure the difference with respect to the reference sequence each time.
-1
0
1
2
3
4
5
1 2 3 4 5 6 7 8 9 10Iterations
Sco
res
Correlogram Score DP Score
Synthetic Data Experiments…Contd.
Replace an amino acid at different location and measure the difference with respect to the reference sequence each time.
-1
0
1
2
3
4
5
1 2 3 4 5 6 7 8 9 10 11 12 13 14Iterations
Sco
res
Correlogram Score DP Score
Synthetic Data Experiments…Contd.
Add an amino acid at different location and measure the difference with respect to the reference sequence each time.
-1
0
1
2
3
4
5
1 2 3 4 5 6 7 8 9 10 11 12 13 14Iterations
Sco
res
Correlogram Score DP Score
Finding Test data..
“Alternate circulation of recent equine-2 influenza viruses (H3N8) from two distinct lineages in the United States” By Alexander C.K. Lai, Kristin M. Rogers, Amy Glaser, Lynn Tudor, Thomas Chambers
hemagglutinin (HA) gene from Different strains of equine-2 influenza viruses.
GeneTool version 1.1. – Compilation and analysis
Phylogenetic analysis was performed by using the deduced HA1 amino acid sequence and the PHYLIP software package
Distance matrix was calculated by using the PROTDIST program, and an unrooted tree generated by using the FITCH program.
Test Data
Phylogeny Tree
Experiment 1 : Using same Test data
We have done an experiment with the same test data.
All the protein sequences were searched. http://www.ebi.ac.uk/cgi-bin/expasyfetch
A distance matrix was created using correlogram distances for every pair among these sequences.
From this distance matrix, a tree is created using PHYLIP software package.
The program ‘FITCH’ is used for creating tree whereas the program ‘DRAWTREE’ is used for visualizing the tree.
Graphical Representation of Correlogram for SA90
0
0.05
0.1
ACDE FGH I KLM NPQRS TVWYA
F
K
P
T
Distance = 0
0
0.01
0.02
ACDE FGH I KLM NPQRS TVWYA
F
K
P
T
Distance = 1
0
0.01
0.02
ACDE FGH I KLM NPQRS TVWYA
F
K
P
T
Distance = 2
Graphical Representation of Correlogram for SA90
0
0.005
0.01
0.015
ACDE FGH I KLM NPQRS TVWYA
F
K
P
T
Distance = 4
0
0.005
0.01
0.015
ACDE FGH I KLM NPQRS TVWYA
F
K
P
T
Distance = 3
Distance Matrix
SA90 SU89 LM92 HK92 KY92 KY91 KY94
SA90 0 0.084172 0.035637 0.087184 0.085504 0.085942 0.086551
SU90 0.084172 0 0.082183 0.014866 0.020469 0.021679 0.020881
LM92 0.035637 0.082183 0 0.081841 0.085076 0.085575 0.085744
HK92 0.087184 0.014866 0.081841 0 0.024637 0.026439 0.025417
KY92 0.085504 0.020469 0.085076 0.024637 0 0.018841 0.017493
KY91 0.085942 0.021679 0.085575 0.026439 0.018841 0 0.016823
KY94 0.086551 0.020881 0.085744 0.025417 0.017493 0.016823 0
Phylogeny Tree found with Correlogram Distances
Comparison of two trees.
Experiment 2 : Finding Test Data
Parvovirus causes stomach diseases in children.
Coat protein – Some coat proteins are important as they are responsible for the resistance.
Different strains of parvoviri were studied for their VP1 Protein.
Reference for the test data – Dr. Mavis McKenna and Dr. Rob McKenna from University of Florida, Gainesville.
From these distance matrices, trees were created using PHYLIP software package.
The programs ‘NEIGHBOR’ and ‘DRAWTREE’ were used.
Comparison of two trees.
Experiment 3 -Correlogram for Sequence Scanning
The next experiment was to use correlogram for scanning Sequences i.e. Pattern Finding.The algorithm Scan Correlogram was developed for finding the occurrences of a given pattern over a long sequence.
2nd Comparison
A T C G T
A T C G A T C G T T A G C T C C
Pattern
Target1st Comparison
Last Comparison
Experiment 3 -Correlogram for Sequence Scanning…Contd.
Following Viruses were used in this experimentPorcine-parvovirusBovine ParvovirusCPV Packaged StrandH1 ComplementaryMVM Packaged StrandPhiX-GenomeAAV NC001401AAV ComplementaryADV ComplementaryAstell and Tattersall MVMi Packaged Sequence
Experiment 3 -Correlogram for Sequence Scanning…Contd.
The patterns searched were as followsACACCAAAAATACCTCTTGCATCCTCTATCAC
Results for Bovine Parvovirus
Following are the results shown for Bovine Parvovirus.The length of sequence was 5517 and cut-off score used was 2.48 for all three patterns.
Pattern 1 - ACACCAAAA
0
0.5
1
1.5
2
2.5
3
0 1000 2000 3000 4000 5000 6000
Location of Substring
Dif
fere
nce S
co
re
Results for Bovine Parvovirus
Following are the results shown for Bovine Parvovirus for pattern ACACCAAAA.
Location Score Distance Substring
129 2.28 ACAACTAAA 2167 1.99 ACCCAAATA3543 2.39 AACTCCAAA4149 1.83 TACCACCAA 4150 1.83 ACCACCAAA 4151 2.09 CCACCAAAT 4152 1.81 CACCAAATC 4798 2.48 ACCCCCAAT
Conclusions??
This research developed the correlogram comparison method for comparing sequences. Experiments were performed on real sequences and on synthetic sequences to answer the research questions of whether the correlogram biological sequences.
It was observed that the Dynamic Programming method was more sensitive to the positioning of characters (i.e. amino acids or nucleic acids) in the sequence (sequence alignment), whereas the Correlogram method was found to be more sensitive to the character itself (contents of the sequence)
Conclusions??
The real data experiment was conducted on different strains of the horse influenza virus and the parvovirus. It was observed that the phylogeny was retained in most cases, however there were certain remarkable differences between the two.
The scan correlogram algorithm was developed and used in this research to find motifs or patterns. The results of this experiment showed that the sub-sequences obtained were very similar to the given pattern.
Future Work
The further study can be done to see how the array of distances used for correlogram computations can impact the results.
It will be interesting to study various delta values for Gapped correlograms and how they affect the scores. This gapped correlogram method can be further researched to see if the delta values are useful in determining global versus local alignments.
Future Work…Contd.
Enhancements can be made to the scan correlogram method to use the gapped correlogram method for finding patterns and also to find the sub-sequences of more or less length than that of the pattern sequence.
Acknowledgement
Dr. Kuntal Sengupta suggested that correlogram method can be used for comparison of bio-sequences.
Dr. Mavis McKenna and Dr. Rob McKenna, University of Florida, Gainesville.
Mridula Anand, Florida Institute of Technology.
References
http://www.ncbi.nlm.nih.gov/BLAST/http://highwire.stanford.edu/http://au.expasy.org/http://evolution.gs.washington.edu/phylip.html“Alternate circulation of recent equine-2 influenza viruses (H3N8) from two distinct lineages in the United States” By Alexander C.K. Lai, Kristin M. Rogers, Amy Glaser, Lynn Tudor, Thomas Chambers.“Image indexing using color correlograms” By Jing Huang,S Ravi
Kumar, Mandar Mitra, Wei-Jing Zhu, Ramin Zabih“Phylogeny of the genus Haemophilus as determined by comparison of partial infB sequences” By Jakob Hedegaard, Henrik Okkels, Brita Bruun, Mogens Kilian, Kim K. Mortensen1 and Niels Nørskov-Lauritsen
Thanks!!
top related