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11.
Augustin Mico 《Commonwealth Law Bulletin》2013,39(3):435-442
Producing law which is clear and easily accessible to the reader is a priority for the drafter. Thus, the use of plain language is one key issue which can help to improve clarity in drafting law. It can make the law much easier to understand and can maintain good standards. At the level of structure, plain language drafters try to organise laws in a clear and meaningful way. If everybody decides to use language in any way he or she likes, it would be impossible to meet the requirements of every listener and reader. 相似文献
12.
Online reference database of European Y-chromosomal short tandem repeat (STR) haplotypes 总被引:9,自引:0,他引:9
Roewer L Krawczak M Willuweit S Nagy M Alves C Amorim A Anslinger K Augustin C Betz A Bosch E Cagliá A Carracedo A Corach D Dekairelle AF Dobosz T Dupuy BM Füredi S Gehrig C Gusmaõ L Henke J Henke L Hidding M Hohoff C Hoste B Jobling MA Kärgel HJ de Knijff P Lessig R Liebeherr E Lorente M Martínez-Jarreta B Nievas P Nowak M Parson W Pascali VL Penacino G Ploski R Rolf B Sala A Schmidt U Schmitt C Schneider PM Szibor R Teifel-Greding J Kayser M 《Forensic science international》2001,118(2-3):106-113
The reference database of highly informative Y-chromosomal short tandem repeat (STR) haplotypes (YHRD), available online at http://ystr.charite.de, represents the largest collection of male-specific genetic profiles currently available for European populations. By September 2000, YHRD contained 4688 9-locus (so-called "minimal") haplotypes, 40% of which have been extended further to include two additional loci. Establishment of YHRD has been facilitated by the joint efforts of 31 forensic and anthropological institutions. All contributing laboratories have agreed to standardize their Y-STR haplotyping protocols and to participate in a quality assurance exercise prior to the inclusion of any data. In view of its collaborative character, and in order to put YHRD to its intended use, viz. the support of forensic caseworkers in their routine decision-making process, the database has been made publicly available via the Internet in February 2000. Online searches for complete or partial Y-STR haplotypes from evidentiary or non-probative material can be performed on a non-commercial basis, and yield observed haplotype counts as well as extrapolated population frequency estimates. In addition, the YHRD website provides information about the quality control test, genotyping protocols, haplotype formats and informativity, population genetic analysis, literature references, and a list of contact addresses of the contributing laboratories. 相似文献
13.
Wittig H Augustin C Baasner A Bulnheim U Dimo-Simonin N Edelmann J Hering S Jung S Lutz S Michael M Parson W Poetsch M Schneider PM Weichhold G Krause D 《Forensic science international》2000,113(1-3):113-118
Sequencing of mtDNA is an advanced method for the individualisation of traces. Disadvantages of this method are expensive and time-consuming analysis and evaluation procedures as well as the necessary stock of population-genetic data which is still insufficient. Central European institutes of forensic medicine from Germany, Austria, and Switzerland have been working together since the beginning of 1998 to establish a mtDNA database. The aim is to build up a large stock of forensically established data and provide population-genetic data for frequency investigations, which will serve as a basis for expert opinions and scientific research. Good data quality is ensured by using original sequences only. Ring tests, which have been conducted to enhance analytical reliability, revealed a high correspondence rate of the analytical results obtained by the individual member institutes. Today 1410 sequences are available for comparison, of which 1285 sequences in the HV1 and HV2 regions cover the full ranges from 16051 to 16365 and from 73 to 340 (according to Anderson). The major part is formed by Central European sequences comprising 1256 data sets from Germany, Austria, and Switzerland. Today the database contains sequences from a total of 12 European, six African and three Asian countries including 100 sequences from Japan. This paper is aimed at discussing the individualisation potentials of mtDNA as well as the possibilities and limits of ethnic differentiation by means of pairwise sequence differences on the basis of the data stock available. 相似文献
14.
Augustin Kwasi Fosu 《发展研究杂志》2013,49(5):726-745
This study explores the extent to which inequality affects the impact of income growth on the rates of poverty changes in sub-Saharan Africa (SSA) compared to non-SSA, based on an unbalanced panel of 86 countries over 1977–2004. For all three measures of poverty – headcount, gap, and squared gap – the impact of GDP growth on poverty reduction is a decreasing function of initial inequality. The impacts are similar in direction for SSA and non-SSA, so that within both regions there are considerable disparities in the responsiveness of poverty to income growth, depending on inequality. Nevertheless, the income–growth elasticity is substantially less for SSA, implying relatively small poverty-reduction response to growth. 相似文献