The effect of whole genome amplification on samples originating from more than one donor

Publikation: Bidrag til bog/antologi/rapportKonferencebidrag i proceedingsForskningfagfællebedømt

Standard

The effect of whole genome amplification on samples originating from more than one donor. / Thacker, C.R.; Balogh, M.K.; Børsting, Claus; Ramos, E.; Sanchez, Diz P.; Carracedo, A.; Morling, N.; Schneider, Peter M.; Syndercombe-Court, Denise; SNPforID Consortium.

Progress in Forensic Genetics 11: Proceedings of the 21st International ISFG Congress. Bind 1288 Elsevier, 2006. s. 722-724 (ICS - International Congress Series).

Publikation: Bidrag til bog/antologi/rapportKonferencebidrag i proceedingsForskningfagfællebedømt

Harvard

Thacker, CR, Balogh, MK, Børsting, C, Ramos, E, Sanchez, DP, Carracedo, A, Morling, N, Schneider, PM, Syndercombe-Court, D & SNPforID Consortium 2006, The effect of whole genome amplification on samples originating from more than one donor. i Progress in Forensic Genetics 11: Proceedings of the 21st International ISFG Congress. bind 1288, Elsevier, ICS - International Congress Series, s. 722-724, Progress in Forensic Genetics 11 - Proceedings of the 21st International ISFG Congress, Ponta Delgada, The Azores, Portugal, 13/09/2005. https://doi.org/doi:10.1016/j.ics.2005.09.170

APA

Thacker, C. R., Balogh, M. K., Børsting, C., Ramos, E., Sanchez, D. P., Carracedo, A., Morling, N., Schneider, P. M., Syndercombe-Court, D., & SNPforID Consortium (2006). The effect of whole genome amplification on samples originating from more than one donor. I Progress in Forensic Genetics 11: Proceedings of the 21st International ISFG Congress (Bind 1288, s. 722-724). Elsevier. ICS - International Congress Series https://doi.org/doi:10.1016/j.ics.2005.09.170

Vancouver

Thacker CR, Balogh MK, Børsting C, Ramos E, Sanchez DP, Carracedo A o.a. The effect of whole genome amplification on samples originating from more than one donor. I Progress in Forensic Genetics 11: Proceedings of the 21st International ISFG Congress. Bind 1288. Elsevier. 2006. s. 722-724. (ICS - International Congress Series). https://doi.org/doi:10.1016/j.ics.2005.09.170

Author

Thacker, C.R. ; Balogh, M.K. ; Børsting, Claus ; Ramos, E. ; Sanchez, Diz P. ; Carracedo, A. ; Morling, N. ; Schneider, Peter M. ; Syndercombe-Court, Denise ; SNPforID Consortium. / The effect of whole genome amplification on samples originating from more than one donor. Progress in Forensic Genetics 11: Proceedings of the 21st International ISFG Congress. Bind 1288 Elsevier, 2006. s. 722-724 (ICS - International Congress Series).

Bibtex

@inproceedings{8297bc3022c811df8ed1000ea68e967b,
title = "The effect of whole genome amplification on samples originating from more than one donor",
abstract = "In this study, the GenomiPhi(TM) DNA Amplification Kit (Amersham Biosciences) was used to investigate the potential of whole genome amplification (WGA) when considering samples originating from more than one donor. DNA was extracted from blood samples, quantified and normalised before being mixed in ratios of 1:1, 1:3, 1:7 and 1:15. Proportions were checked using standard STR analysis before being subjected to WGA. Once amplified using GenomiPhi(TM), the ratios were again checked. Relative proportions were found to be maintained in the 1:1 and 1:3 ratios following WGA; the observed peak ratios were found to match the expected peak ratios regardless of the starting concentration of DNA. With samples mixed in the ratio of 1:7 and 1:15, and when the concentration of starting material was at the manufacturer's lower limit, too few minor component peaks were found to allow for statistical analysis. With an initial template exceeding 1 ng/[mu]L there was an increase in problems associated with profile interpretation but the results obtained indicated that mixture proportions could be quantifiably maintained",
author = "C.R. Thacker and M.K. Balogh and Claus B{\o}rsting and E. Ramos and Sanchez, {Diz P.} and A. Carracedo and N. Morling and Schneider, {Peter M.} and Denise Syndercombe-Court and {SNPforID Consortium}",
year = "2006",
doi = "doi:10.1016/j.ics.2005.09.170",
language = "English",
volume = "1288",
series = "ICS - International Congress Series",
publisher = "Elsevier",
pages = "722--724",
booktitle = "Progress in Forensic Genetics 11",
address = "Netherlands",
note = "null ; Conference date: 13-09-2005 Through 16-09-2005",

}

RIS

TY - GEN

T1 - The effect of whole genome amplification on samples originating from more than one donor

AU - Thacker, C.R.

AU - Balogh, M.K.

AU - Børsting, Claus

AU - Ramos, E.

AU - Sanchez, Diz P.

AU - Carracedo, A.

AU - Morling, N.

AU - Schneider, Peter M.

AU - Syndercombe-Court, Denise

AU - SNPforID Consortium

PY - 2006

Y1 - 2006

N2 - In this study, the GenomiPhi(TM) DNA Amplification Kit (Amersham Biosciences) was used to investigate the potential of whole genome amplification (WGA) when considering samples originating from more than one donor. DNA was extracted from blood samples, quantified and normalised before being mixed in ratios of 1:1, 1:3, 1:7 and 1:15. Proportions were checked using standard STR analysis before being subjected to WGA. Once amplified using GenomiPhi(TM), the ratios were again checked. Relative proportions were found to be maintained in the 1:1 and 1:3 ratios following WGA; the observed peak ratios were found to match the expected peak ratios regardless of the starting concentration of DNA. With samples mixed in the ratio of 1:7 and 1:15, and when the concentration of starting material was at the manufacturer's lower limit, too few minor component peaks were found to allow for statistical analysis. With an initial template exceeding 1 ng/[mu]L there was an increase in problems associated with profile interpretation but the results obtained indicated that mixture proportions could be quantifiably maintained

AB - In this study, the GenomiPhi(TM) DNA Amplification Kit (Amersham Biosciences) was used to investigate the potential of whole genome amplification (WGA) when considering samples originating from more than one donor. DNA was extracted from blood samples, quantified and normalised before being mixed in ratios of 1:1, 1:3, 1:7 and 1:15. Proportions were checked using standard STR analysis before being subjected to WGA. Once amplified using GenomiPhi(TM), the ratios were again checked. Relative proportions were found to be maintained in the 1:1 and 1:3 ratios following WGA; the observed peak ratios were found to match the expected peak ratios regardless of the starting concentration of DNA. With samples mixed in the ratio of 1:7 and 1:15, and when the concentration of starting material was at the manufacturer's lower limit, too few minor component peaks were found to allow for statistical analysis. With an initial template exceeding 1 ng/[mu]L there was an increase in problems associated with profile interpretation but the results obtained indicated that mixture proportions could be quantifiably maintained

U2 - doi:10.1016/j.ics.2005.09.170

DO - doi:10.1016/j.ics.2005.09.170

M3 - Article in proceedings

VL - 1288

T3 - ICS - International Congress Series

SP - 722

EP - 724

BT - Progress in Forensic Genetics 11

PB - Elsevier

Y2 - 13 September 2005 through 16 September 2005

ER -

ID: 18251470