sgSNP 377 Contig21552 sgSNP 247 Contig11105 sgSNP 1433 Contig10821

Slides:



Advertisements
Similar presentations
C e / mol/L q e / mol/g This Journal is © The Royal Society of Chemistry 2002 Figure.
Advertisements

Supplemental Figure 1 A No. at risk T T T
Polymorphisms: Clinical Implications By Amr S. Moustafa, M.D.; Ph.D. Assistant Prof. & Consultant, Medical Biochemistry Dept. College of Medicine, KSU.
Shape of DATA. How would you describe the shape of this graph?
RNA Lab (Isolation, quantification and qPCR analysis) MCB7300.
Figure 6.04 Effect of a catalyst on a chemical reaction.
P247. Figure 9-1 p248 Figure 9-2 p251 p251 Figure 9-3 p253.
IGEM 101: Session 6 4/9/15Jarrod Shilts 4/11/15Ophir Ospovat.
Graph-to-Text How to write well about a graphical instrument?
Quantification of RNA by real-time PCR
Chapter 08 Author: Kelly Elkins © 2013 Elsevier, Inc. All rights reserved.
-11.9 kb -4.2 kb -5.6 kb Gfi1 +/1b neo Gfi1 +/+ Gfi1 +/1b Gfi1 1b/1b Gfi1 +/1b Gfi1 +/ kb kb Gfi1 +/+ Gfi1 +/1b -14 kb - 8 kb B A Gfi1 +/+
What is a Phase diagram? Phase diagram: plot of pressure vs. Temperature summarizing all equilibria between phases. Given a temperature and pressure, phase.
PRINC E TON School of Engineering and Applied Science Characterizing Mathematical Models for Polymerase Chain Reaction Kinetics Ifunanya Nwogbaga, Henry.
PCR conditions: 94ºC for 15 min
Date of download: 10/17/2017 Copyright © ASME. All rights reserved.
A Melting Curve Analysis–Based PCR Assay for One-Step Genotyping of β- Thalassemia Mutations  Fu Xiong, Qiuying Huang, Xiaoyun Chen, Yuqiu Zhou, Xinhua.
Keyur P. Patel, Bedia A. Barkoh, Zhao Chen, Deqin Ma, Neelima Reddy, L
Date of download: 10/23/2017 Copyright © ASME. All rights reserved.
Figure 1. Representative mismatched amplification mutation assay polymerase chain reaction amplicons for detection of 16u>c rrs mutation in 14 Mycobacterium.
Figure 6.2 Comparison among the Debye heat capacity, the Einstein heat capacity, and the actual heat capacity of aluminum.
EPP Peak #1 Extraction 1 Extraction 2 Extraction 3 Gel 1 Gel 2
© 2013 Elsevier, Inc. All rights reserved.
Simultaneous Genotyping of α-Thalassemia Deletional and Nondeletional Mutations by Real-Time PCR–Based Multicolor Melting Curve Analysis  Qiuying Huang,
One-Step Ligation on RNA Amplification for the Detection of Point Mutations  Lei Zhang, Jingjing Wang, Mia Coetzer, Stephanie Angione, Rami Kantor, Anubhav.
Applications of the Derivative
Locked Nucleic Acids Can Enhance the Analytical Performance of Quantitative Methylation-Specific Polymerase Chain Reaction  Karen S. Gustafson  The Journal.
Derivative of a Function
© 2013 Elsevier, Inc. All rights reserved.
© 2013 Elsevier, Inc. All rights reserved.
Minimal Residual Disease Monitoring of Acute Myeloid Leukemia by Massively Multiplex Digital PCR in Patients with NPM1 Mutations  Nuria Mencia-Trinchant,
الفعل ورد الفعل ♠ ♠ ♠ مجلس أبوظبي للتعليم منطقة العين التعليمية
DNA fragmentation of human sperm can be detected by ligation-mediated real-time polymerase chain reaction  Jung Jin Lim, Ph.D., Jin Il Lee, M.Sc., Dong.
Molecular Analysis of Circulating Cell-Free DNA from Lung Cancer Patients in Routine Laboratory Practice  Stephan Bartels, Sascha Persing, Britta Hasemeier,
A Melting Curve Analysis–Based PCR Assay for One-Step Genotyping of β- Thalassemia Mutations  Fu Xiong, Qiuying Huang, Xiaoyun Chen, Yuqiu Zhou, Xinhua.
Single Nucleotide Polymorphism-Based System Improves the Applicability of Quantitative PCR for Chimerism Monitoring  Egle Gineikiene, Mindaugas Stoskus,
A Novel Targeted Approach for Noninvasive Detection of Paternally Inherited Mutations in Maternal Plasma  Jessica M.E. van den Oever, Ivonne J.H.M. van.
RET Proto-Oncogene Genotyping Using Unlabeled Probes, the Masking Technique, and Amplicon High-Resolution Melting Analysis  Rebecca L. Margraf, Rong Mao,
Cornelis J. J. Huijsmans, Jeroen Poodt, Paul H. M. Savelkoul, Mirjam H
Long-Range (17.7 kb) Allele-Specific Polymerase Chain Reaction Method for Direct Haplotyping of R117H and IVS-8 Mutations of the Cystic Fibrosis Transmembrane.
Understanding Supply.
Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal.
Teresa Almeida Santos, Ph. D. , Shahy El Shourbagy, M. D. , Justin C
Neuropotency of Human Mesenchymal Stem Cell Cultures: Clonal Studies Reveal the Contribution of Cell Plasticity and Cell Contamination  Rodrigo Somoza,
Simultaneous Genotyping of α-Thalassemia Deletional and Nondeletional Mutations by Real-Time PCR–Based Multicolor Melting Curve Analysis  Qiuying Huang,
Specific Detection of Cytokeratin 20-Positive Cells in Blood of Colorectal and Breast Cancer Patients by a High Sensitivity Real-Time Reverse Transcriptase-Polymerase.
Pol alpha (Row B) Amplification Plots
EDLC(Embedded system Development Life Cycle ).
Rapid Detection of Clonal T-Cell Receptor-β Gene Rearrangements in T-Cell Lymphomas Using the LightCycler-Polymerase Chain Reaction with DNA Melting Curve.
A) B) C) Derivative reporter (-Rn) Temperature (°C) Temperature (°C)
Supplemental Figure 1. Supplemental Figure 1. Schematic flow chart of patient enrollment.
Analytical Detection of Immunoglobulin Heavy Chain Gene Rearrangements in Gastric Lymphoid Infiltrates by Peak Area Analysis of the Melting Curve in the.
Keyur P. Patel, Bedia A. Barkoh, Zhao Chen, Deqin Ma, Neelima Reddy, L
Christine Formisano-Tréziny, Marina de San Feliciano, Jean Gabert 
KRAS Mutation The Journal of Molecular Diagnostics
A novel method for the rapid and prospective identification of Beijing Mycobacterium tuberculosis strains by high-resolution melting analysis  M. Alonso,
Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays  Nathan R. Treff,
Efficient and Highly Sensitive Screen for Myotonic Dystrophy Type 1 Using a One-Step Triplet-Primed PCR and Melting Curve Assay  Mulias Lian, Indhu-Shree.
Quantitative and Qualitative Analyses of the SNRPN Gene Using Real-Time PCR with Melting Curve Analysis  Chia-Cheng Hung, Shin-Yu Lin, Shuan-Pei Lin,
Multiplexed High Resolution Melting Assay for Versatile Sample Tracking in a Diagnostic and Research Setting  Céline Helsmoortel, R. Frank Kooy, Geert.
Larissa V. Furtado, Helmut C. Weigelin, Kojo S. J
Diagnosis of Human Congenital Cytomegalovirus Infection by Amplification of Viral DNA from Dried Blood Spots on Perinatal Cards  Lori Scanga, Shu Chaing,
Low Incidence of Minor BRAF V600 Mutation-Positive Subclones in Primary and Metastatic Melanoma Determined by Sensitive and Quantitative Real-Time PCR 
Enthalpy and Phase Changes
Pol alpha Amplification Plots
Definite Integrals 5.6 Area Between Curves.
Improved Detection of the KIT D816V Mutation in Patients with Systemic Mastocytosis Using a Quantitative and Highly Sensitive Real-Time qPCR Assay  Thomas.
GRAPHICAL DETERMINATION OF ΔHº AND ΔSº
Amplification curve from the MeVA RT-qPCR on the Roche LightCycler 480 system. Amplification curve from the MeVA RT-qPCR on the Roche LightCycler 480 system.
Presentation transcript:

sgSNP 377 Contig21552 sgSNP 247 Contig11105 sgSNP 1433 Contig10821 Reference reaction Reaction with allele 1 Reaction with allele 2 2.0 1.5 1.0 sgSNP 377 Contig21552 0.5 65.0 75.0 80.0 85.0 90.0 95.0 70.0 0.8 0.6 0.4 0.2 sgSNP 247 Contig11105 0.0 65.0 75.0 80.0 85.0 90.0 95.0 70.0 1.6 1.4 1.2 1.0 0.8 0.6 sgSNP 1433 Contig10821 0.4 0.2 65.0 70.0 75.0 80.0 85.0 90.0 95.0 1.5 1.3 1.1 0.9 0.7 sgSNP 193 Contig10284 0.5 0.3 0.1 65.0 70.0 75.0 80.0 85.0 90.0 95.0 1.6 1.4 1.2 1.0 0.8 0.6 0.4 sgSNP 521 Contig 17875 0.2 65.0 70.0 75.0 80.0 85.0 90.0 95.0 65.0 75.0 80.0 85.0 90.0 95.0 70.0 1.4 1.2 1.0 0.6 0.4 0.8 0.2 sgSNP 1297 Contig18072 Supplemental Figure S6. Amplification plot (left) and melting curve (right) of sgSNPs by qPCR. The amplification graphics show the ΔRn during the cycles reaction to different reactions (reference reaction, reaction with allele 1 and reaction with allele 2). The melting curve graphic shows the representation of derivative reporter (-Rn) during increase of temperature and the formation of only one peak showing that the reaction had specific amplification.