(Q36627902)

15 August 2017

Whole genome amplification of degraded and nondegraded DNA for forensic purposes (English)

1 reference

15 August 2017

whole genome sequencing

1 reference

inferred from title

author name string

Agnieszka Maciejewska

series ordinal

1

1 reference

15 August 2017

Joanna Jakubowska

series ordinal

2

1 reference

15 August 2017

Ryszard Pawłowski

series ordinal

3

1 reference

15 August 2017

1 September 2012

1 reference

International Journal of Legal Medicine

15 August 2017

1 reference

15 August 2017

127

1 reference

15 August 2017

2

1 reference

15 August 2017

309-319

1 reference

https://scigraph.springernature.com/pub.10.1007/s00414-012-0764-9

15 August 2017

0 references

cites work

Validity of low copy number typing and applications to forensic science

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Whole genome amplification of plasma-circulating DNA enables expanded screening for allelic imbalance in plasma

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Exploring whole genome amplification as a DNA recovery tool for molecular genetic studies.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

The use of whole genome amplification in the study of human disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

DNA amplification method tolerant to sample degradation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Whole-genome amplification of DNA from residual cells left by incidental contact

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Comprehensive human genome amplification using multiple displacement amplification

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

A human mitochondrial DNA standard reference material for quality control in forensic identification, medical diagnosis, and mutation detection

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Multiple mutation analyses in single tumor cells with improved whole genome amplification

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Mutation detection and single-molecule counting using isothermal rolling-circle amplification

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Reliable genotyping of samples with very low DNA quantities using PCR.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Whole genome amplification from a single cell: implications for genetic analysis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

Application of mtDNA sequence analysis in forensic casework for the identification of human remains

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578730

An investigation of the rigor of interpretation rules for STRs derived from less than 100 pg of DNA.

28 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00414-012-0764-9

Comparison of two whole genome amplification methods for STR genotyping of LCN and degraded DNA samples.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00414-012-0764-9

The utility of whole genome amplification for typing compromised forensic samples.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00414-012-0764-9

Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00414-012-0764-9

Evaluation of circular DNA substrates for whole genome amplification prior to forensic analysis

21 January 2018

1 reference

12 December 2020

Forensic validation of a multiplex containing nine STRs--population genetics in northern Poland

1 reference

12 December 2020

Fetal origin of single nucleated erythroblasts and free DNA in the peripheral blood of pregnant women

1 reference

12 December 2020

Identification of human remains by amplification and automated sequencing of mitochondrial DNA

1 reference

12 December 2020

Frequencies for five short tandem repeat (STR) systems in a population from north Poland

1 reference

12 December 2020

Whole-genome amplification: relative efficiencies of the current methods

1 reference

12 December 2020

Whole genome amplification strategy for forensic genetic analysis using single or few cell equivalents of genomic DNA

1 reference

12 December 2020

10.1007/S00414-012-0764-9

Identifiers

DOI

1 reference

15 August 2017

1 reference

15 August 2017

PubMed publication ID

22940764

1 reference