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1
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43049120073
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The STRbase website lists a wide range of observed STR mutation rates at: http://www.cstl.nist.gov/biotech/strbase/mutation.htm based on data from the most extensive recent AABB survey, typing trios with standard STRs, outlined at: http://www.aabb.org/Documents/Accreditation/Parentage_Testing_Accreditation_Program/ptannrpt03.pdf
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The STRbase website lists a wide range of observed STR mutation rates at: http://www.cstl.nist.gov/biotech/strbase/mutation.htm based on data from the most extensive recent AABB survey, typing trios with standard STRs, outlined at: http://www.aabb.org/Documents/Accreditation/Parentage_Testing_Accreditation_Program/ptannrpt03.pdf
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2
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0031778070
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Mutation rates in human microsatellites: influence of the structure and length of the tandem repeat
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Brinkman B., Klintshar M., Neuhuber F., Hühne J., and Rolf B. Mutation rates in human microsatellites: influence of the structure and length of the tandem repeat. Am. J. Hum. Genet. 62 (1998) 1408-1415
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Klintshar, M.2
Neuhuber, F.3
Hühne, J.4
Rolf, B.5
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3
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43049099404
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A regularly updated catalogue of STR null alleles reported in the literature is maintained at STRbase: http://www.cstl.nist.gov/biotech/strbase/NullAlleles.htm
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A regularly updated catalogue of STR null alleles reported in the literature is maintained at STRbase: http://www.cstl.nist.gov/biotech/strbase/NullAlleles.htm
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6
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0033730752
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Promega corporation reveals primer sequences in its testing kits
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Mosibay A., Mozer T.J., and Sprecher C. Promega corporation reveals primer sequences in its testing kits. J. Forensic Sci. 45 (2000) 1360-1362
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Mosibay, A.1
Mozer, T.J.2
Sprecher, C.3
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7
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0031857103
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Sequence variation of a hypervariable short tandem repeat at the D1S1656 locus
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Lareu M.V., Barral S., Salas A., Pestoni C., and Carracedo A. Sequence variation of a hypervariable short tandem repeat at the D1S1656 locus. Int. J. Legal Med. 111 (1998) 244-247
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Lareu, M.V.1
Barral, S.2
Salas, A.3
Pestoni, C.4
Carracedo, A.5
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8
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0030571519
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Sequence variation of a hypervariable short tandem repeat at the D12S391 locus
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Lareu M.V., Pestoni C., Barros F., Salas A., and Carracedo A. Sequence variation of a hypervariable short tandem repeat at the D12S391 locus. Gene 182 (1996) 151-153
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Lareu, M.V.1
Pestoni, C.2
Barros, F.3
Salas, A.4
Carracedo, A.5
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9
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0031754274
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Sequence variation of a variable short tandem repeat at the D18S535 locus
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Lareu M.V., Barral S., Salas A., and Carracedo A. Sequence variation of a variable short tandem repeat at the D18S535 locus. Int. J. Legal Med. 111 (1998) 337-339
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Lareu, M.V.1
Barral, S.2
Salas, A.3
Carracedo, A.4
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10
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33646557707
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A multiplex assay with 52 single nucleotide polymorphisms for human identification
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Sánchez J.J., Phillips C., Børsting C., Balogh K., Bogus M., Fondevila M., Harrison C.D., Musgrave-Brown E., Salas A., Syndercombe Court D., Schneider P.M., Carracedo A., and Morling N. A multiplex assay with 52 single nucleotide polymorphisms for human identification. Electrophoresis 27 (2006) 1713-1724
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Sánchez, J.J.1
Phillips, C.2
Børsting, C.3
Balogh, K.4
Bogus, M.5
Fondevila, M.6
Harrison, C.D.7
Musgrave-Brown, E.8
Salas, A.9
Syndercombe Court, D.10
Schneider, P.M.11
Carracedo, A.12
Morling, N.13
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11
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43049083421
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Challenging DNA: assessment of a range of genotyping approaches for highly degraded forensic samples
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(in publication)
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Fondevila M., Phillips C., Naverán N., Cerezo M., Rodríguez A., Calvo R., Fernández L.M., Carracedo A., and Lareu M.V. Challenging DNA: assessment of a range of genotyping approaches for highly degraded forensic samples. Prog. Forensic Genet. 12 (2008) (in publication)
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Fondevila, M.1
Phillips, C.2
Naverán, N.3
Cerezo, M.4
Rodríguez, A.5
Calvo, R.6
Fernández, L.M.7
Carracedo, A.8
Lareu, M.V.9
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12
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43049088159
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Identification of skeletal remains using short-amplicon marker analysis of severely degraded DNA extracted from a decomposed and charred femur
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Fondevila M., Phillips C., Naveran N., Fernández L., Cerezo M., Salas A., Carracedo A., and Lareu M.V. Identification of skeletal remains using short-amplicon marker analysis of severely degraded DNA extracted from a decomposed and charred femur. Forensic Sci. Int. Genet. 2 (2008) 212-218
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Fondevila, M.1
Phillips, C.2
Naveran, N.3
Fernández, L.4
Cerezo, M.5
Salas, A.6
Carracedo, A.7
Lareu, M.V.8
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13
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34249094940
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The SNPforID Consortium, Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel
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Phillips C., Fang R., Ballard D., Fondevila M., Harrison C., Hyland F., Musgrave-Brown E., Proff C., Ramos-Luis E., Sobrino B., Furtado M., Syndercombe Court D., Carracedo A., and Schneider P.M. The SNPforID Consortium, Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel. Forensic Sci. Int. Genet. 1 (2007) 180-185
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Phillips, C.1
Fang, R.2
Ballard, D.3
Fondevila, M.4
Harrison, C.5
Hyland, F.6
Musgrave-Brown, E.7
Proff, C.8
Ramos-Luis, E.9
Sobrino, B.10
Furtado, M.11
Syndercombe Court, D.12
Carracedo, A.13
Schneider, P.M.14
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14
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0034621283
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Beyond traditional paternity and identification cases. Selecting the most probable pedigree
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Egeland T., Mostad P., Mevåg B., and Stenersen M. Beyond traditional paternity and identification cases. Selecting the most probable pedigree. Forensic Sci. Int. 110 (2000) 47-59
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Egeland, T.1
Mostad, P.2
Mevåg, B.3
Stenersen, M.4
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15
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43049115022
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Comparison of paternity indices based on typing 15 STRs, 7 VNTRs and 52 SNPs in 50 Danish mother-child-father trios
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Børsting C., Sanchez J.J., Birk A.H., Bruun H.Q., Hallenberg C., Hansen A.J., Hansen H.E., Simonsen B.T., and Morling N. Comparison of paternity indices based on typing 15 STRs, 7 VNTRs and 52 SNPs in 50 Danish mother-child-father trios. Prog. Forensic Genet. 11 (2006) 436-438
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, vol.11
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Børsting, C.1
Sanchez, J.J.2
Birk, A.H.3
Bruun, H.Q.4
Hallenberg, C.5
Hansen, A.J.6
Hansen, H.E.7
Simonsen, B.T.8
Morling, N.9
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16
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0033828761
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Estimate of the mutation rate per nucleotide in humans
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Nachman M.W., and Crowell S.L. Estimate of the mutation rate per nucleotide in humans. Genetics 156 (2000) 297-304
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Nachman, M.W.1
Crowell, S.L.2
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