Detection of Labeling Markers on Synthetic DNA molecules
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Detection of Labeling Markers on Synthetic DNA molecules Backgrou nd Deoxyribonucleic acid (DNA) is the “code of life” that provides the recipe of genetic traits to all living organisms. DNA is a sequence of nucleotide base pairs that identify the correct order of amino acids that make up the proteins and end up defining all physical characteristics. A major road block in the effort to study and understand DNA has been sequencing the base pairs. Current sequencing techniques are costly and time intensive ZSGenetics has developed a patented technique to bind larger “heavy” labeling atoms to certain base pairs of DNA. DNA contains relatively “light” atoms (low atomic number). These labeling atoms provide enough contrast to be viewed when imaged using a scanning transmission electron microscope (STEM). With the fundamental development of this labeling technique, finding these markers means finding the particular base pair it was attached to, thus sequencing the DNA by visual means. Nathan P. Brouwer •ECE Department •Hamel Center for Undergraduate Research •Professor Richard A. Messner •William Glover, ZSGenetics Advisor: Richard A. Messner Example Raw Image and Manual Identification of DNA (Annular Dark Field Imaging- Raster Scanned) This research is ground work for the automatic detection and sequencing of human and other genomes. By taking an image of specially prepared DNA samples and using intelligently prepared image processing algorithms, we can drastically cut time and money required to sequence long DNA chains. If successful, it will undoubtedly cause an explosion of research into genetic traits and variations. The implications in the medical field are profound. Future scientists and researchers could work towards understanding and curing genetic defects and diseases. Implication s Project Continuation I plan to continue this project by attempting higher level image processing algorithms and approaches as a master’s thesis while attending graduate school at UNH. ZSGenetics is working on a new ultra thin graphine substrate that shows promise to further reduce noise by increasing contrast. With improved images and additional processing (higher level filters and transforms), it seems very possible to move forward towards automatic detection , identifying periodicity, and directly sequencing the DNA via an imaging process •Accelerates an ionized beam of concentrated electrons onto the sample •Electrons travelling through the sample are deflected due to the positive charge of the nuclei of the atoms in the sample •A Sensitive Detection Mechanism detects the received energy and a pixel is produced for each point in a 2D image lattice STEM Basics Introduction The inherent problem with high resolution STEM images is the high level of back ground noise corruption. Improving the signal to noise ratio to an adequate level is one of the major challenges of this project. ZSGenetics has synthetically created a DNA molecule with every third base pair labeled. This means labels should occur between 1.3nm to 1.75nm apart. Resear ch To get up to speed, background research was necessary to gather fundamental principles from literature and scientific articles in: • DNA Concepts •Electron Microscopy •Image Processing Techniques •Software: ImageJ and MATLAB Approach (ImageJ) The following steps describe the methodology of the approach in ImageJ : Extracted DNA Strand Apply Threshold and Ceiling Manually Cropped about the DNA Cha Zoomed in and added Pseudo Color One Possible String of Marker Atom Cropped Image Imported into MATLAB After preprocessing in ImageJ, the following can be performed using MATLAB: Acknowledgements: Conclusio n It is clear that there is DNA information in the images to be extracted. The labeling markers are providing enough contrast to be detected, but it seems there is still significant noise corruption embedded in the useful information. Extraction algorithms coupled with thresholding and pseudocoloring were used to create the final image useful for human interpretation. It is clear that individual base pairs can be labeled and viewed by these image processing techniques. Future work may make it possible to sequence an entire strand of DNA solely based on its digital image. 3D View of DNA Sequence Nathan P. Brouwer [email protected] Department of Electrical Engineering University of New Hampshire Durham, NH 03824 Approach (MATLAB) The Synthetic Vision and Pattern Analysis Laboratory College of Engineering and Physical Sciences University of New Hampshire
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Nathan P. Brouwer. Advisor: Richard A. Messner. The Synthetic Vision and Pattern Analysis Laboratory. Introduction. Approach (MATLAB). - PowerPoint PPT Presentation
Transcript of Detection of Labeling Markers on Synthetic DNA molecules
Detection of Labeling Markers on Synthetic DNA molecules
Background Deoxyribonucleic acid (DNA) is the “code of life” that provides the recipe of genetic traits to all living organisms. DNA is a sequence of nucleotide base pairs that identify the correct order of amino acids that make up the proteins and end up defining all physical characteristics. A major road block in the effort to study and understand DNA has been sequencing the base pairs. Current sequencing techniques are costly and time intensive ZSGenetics has developed a patented technique to bind larger “heavy” labeling atoms to certain base pairs of DNA. DNA contains relatively “light” atoms (low atomic number). These labeling atoms provide enough contrast to be viewed when imaged using a scanning transmission electron microscope (STEM). With the fundamental development of this labeling technique, finding these markers means finding the particular base pair it was attached to, thus sequencing the DNA by visual means.
Nathan P. Brouwer
•ECE Department•Hamel Center for Undergraduate Research•Professor Richard A. Messner•William Glover, ZSGenetics
Advisor: Richard A. Messner
Example Raw Imageand Manual Identification of DNA
(Annular Dark Field Imaging-Raster Scanned)
This research is ground work for the automatic detection and sequencing of human and other genomes. By taking an image of specially prepared DNA samples and using intelligently prepared image processing algorithms, we can drastically cut time and money required to sequence long DNA chains. If successful, it will undoubtedly cause an explosion of research into genetic traits and variations. The implications in the medical field are profound. Future scientists and researchers could work towards understanding and curing genetic defects and diseases.
Implications
Project Continuation I plan to continue this project by attempting higher level image processing algorithmsand approaches as a master’s thesis while attending graduate school at UNH. ZSGenetics is working on a new ultra thin graphine substrate that shows promise to further reduce noise by increasing contrast. With improved images and additional processing (higher level filters and transforms), it seems very possible to move forward towards automatic detection , identifying periodicity, and directly sequencing the DNA via an imaging process
• Accelerates an ionized beam of concentrated electrons onto the sample
• Electrons travelling through the sample are deflected due to the positive charge of the nuclei of the atoms in the sample
• A Sensitive Detection Mechanism detects the received energy and a pixel is produced for each point in a 2D image lattice
STEM Basics
Introduction The inherent problem with high resolution STEM images is the high level of back ground noise corruption. Improving the signal to noise ratio to an adequate level is one of the major challenges of this project. ZSGenetics has synthetically created a DNA molecule with every third base pair labeled. This means labels should occur between 1.3nm to 1.75nm apart.
ResearchTo get up to speed, background research was necessary to gather fundamental principles from literature and scientific articles in:• DNA Concepts• Electron Microscopy• Image Processing Techniques • Software: ImageJ and MATLAB
Approach (ImageJ) The following steps describe the methodology of the approach in ImageJ :
Extracted DNA Strand
Apply Threshold and Ceiling
Manually Cropped about the DNA Chain
Zoomed in and added Pseudo Color One Possible String of Marker Atoms
Cropped Image Imported into MATLAB
After preprocessing in ImageJ, the following can be performed using MATLAB:
Acknowledgements:
Conclusion It is clear that there is DNA information in the images to be extracted. The labeling markers are providing enough contrast to be detected, but it seems there is still significant noise corruption embedded in the useful information. Extraction algorithms coupled with thresholding and pseudocoloring were used to create the final image useful for human interpretation. It is clear that individual base pairs can be labeled and viewed by these image processing techniques. Future work may make it possible to sequence an entire strand of DNA solely based on its digital image. 3D View of DNA Sequence
Nathan P. [email protected]
Department of Electrical EngineeringUniversity of New Hampshire
Durham, NH 03824
Approach (MATLAB)
The Synthetic Vision and Pattern Analysis Laboratory
College of Engineering and Physical Sciences
University of New Hampshire
