Patent Application
20110269128
1. The Field of the Invention
The present invention is concerned with improvements in and relating to forensic identification, particularly where based on DNA profiling.
2. The Relevant Technology
DNA profiling offers a versatile identification technique for a wide variety of applications including, anthropological, paternity and other forensic environments. The use of such profiling is significant in determining links, or their absence, between samples. Such samples might include those taken from known individuals and/or those taken from the scene of or linked to a crime.
DNA profiling based on the use of short tandem repeats (STR) or micro satellite loci is used in such applications. STR's are a class of polymorphic markers which consist of simple tandomly repeated sequences of between 1 and 6 base pairs in length. STR's in the non-coding part of the genome are generally considered.
In the human genome STR's occur every 6 to 10 kilo bases along the DNA. The length, however, varies greatly between individuals due to mutation and provides identifying characteristics as a result.
A variety of DNA profiling systems exist, including single locus analysis and multiple locus analysis where a number of STR loci are simultaneously amplified.
In analysing the results from an unknown sample it is generally considered against a ladder marker consisting of alleles derived from actual samples. The allelic ladder provides a reference point and allows correspondence of alleles to be identified clearly.
The present invention provides new alleles and new ladders incorporating them for a variety of loci. The present invention offers an improved range and coverage of markers as a result. The ladders include a number of rare alleles offering improved identification of the alleles in an unknown sample.
According to a first aspect of the invention we provide an allelic ladder mixture comprising one or more of the following allelic ladders:
i) an allelic ladder for locus HUMVWFA31/A comprising one or more of alleles comprising or consisting of sequences:
TCTA TCTG TCTA (TCTG)4 (TCTA)3 (SEQ ID NO: 1);
TCTA (TCTG)4 (TCTA)7 (SEQ ID NO: 2); or
(TCTA)2 (TCTG)4 (TCTA)3 TCCA (TCTA)3 (SEQ ID NO: 3) or at least 75% homologous thereto;
ii) an allelic ladder for locus HUMTHOl comprising or consisting of sequence:
(TCAT)4 CAT (TCAT)7 TCGT TCAT (SEQ ID NO: 4); or at least 75% homologous thereto;
iii) an allelic ladder for locus D8S1179 comprising one or more of alleles:
(TCTA)8 (SEQ ID NO: 5);
(TCTA)2 TCTG(TCTA)16 (SEQ ID NO: 6) or at least 75% homologous thereto;
iv) an allelic ladder for locus HUMFIBRA/FGA comprising one or more of alleles comprising or consisting of the sequences:
(TTTC)3 TTTT TTCT (CTTT)5 T (CTTT)3 CTCC (TTCC)2 (SEQ ID NO: 7);
(TTTC)3 TTTT TTCT (CTTT)13 CCTT (CTTT)5 CTCC (TTCC)2 (SEQ ID NO: 8);
(TTTC)3 TTTT TTCT (CTTT)16 CCTT (CTTT)5 CTCC (TTCC)2 (SEQ ID NO: 9);
(TTTC)4 TTTT TT (CTTT)15 (CTTC)3 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 10);
(TTTC)4 TTTT TT (CTTT)16 (CTTC)3 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 11);
(TTTC)4 TTTT TT (CTTT)17 (CTTC)3 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 12);
(TTTC)4 TTTT TT (CTTT)8 (CTGT)4 (CTTT)13 (CTTC)4 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 13);
(TTTC)4 TTTT TT (CTTT)8 (CTGT)5 (CTTT)13 (CTTC)4 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 14);
(TTTC)4 TTTT TT (CTTT)11 (CTGT)3 (CTTT)14 (CTTC)3 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 15);
(TTTC)4 TTTT TT (CTTT)10 (CTGT)5 (CTTT)13 (CTTC)4 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 16);
(TTTC)4 TTTT TT (CTTT)12 (CTGT)5 (CTTT)14 (CTTC)3 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 17); or
(TTTC)4 TTTT TT (CTTT)14 (CTGT)3 (CTTT)14 (CTTC)4 (CTTT)3 CTCC (TTCC)4 (SEQ ID NO: 18); or at least 75% homologous thereto;
v) an allelic ladder for locus D21S11 comprising one or more of alleles comprising or consisting of sequences: (TCTA)4 (TCTG)6 (TCTA)3 TA(TCTA)3 TCA (TCTA)2 TCCATA (TCTA)6 TCGTCT (SEQ ID NO: 19);
(TCTA)5 (TCTG)6 (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)9 TCGTCT (SEQ ID NO: 20);
(TCTA)5 (TCTG)6 (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)10 TCGTCT (SEQ ID NO: 21);
(TCTA)4 (TCTG)6 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)8 TCGTCT (SEQ ID NO: 22);
(TCTA)5 (TCTG)5 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)9 TCGTCT (SEQ ID NO: 23);
(TCTA)4 (TCTG)6 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)10 TCGTCT (SEQ ID NO: 24);
(TCTA)4 (TCTG)6 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)11 TCGTCT (SEQ ID NO: 25);
(TCTA)6 (TCTG)5 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)11 TCGTCT (SEQ ID NO: 26);
(TCTA)5 (TCTG)6 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)12 TCGTCT (SEQ ID NO: 27);
(TCTA)5 (TCTG)6 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)11 TA TCTA TCGTCT (SEQ ID NO: 28);
(TCTA)5 (TCTG)6 (TCTA)3 TA (TCTA)3 TCA (TCTA)3 TCCATA (TCTA)12 TA TCTA TCGTCT (SEQ ID NO: 29);
(TCTA)5 (TCTG)6 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)13 TA TCTA TCGTCT (SEQ ID NO: 30);
(TCTA)5 (TCTG)6 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)14 TATCTA TCGTCT (SEQ ID NO: 31);
(TCTA)10 (TCTG)5 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)12 TCGTCT (SEQ ID NO: 32);
(TCTA)11 (TCTG)5 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)12 TCGTCT (SEQ ID NO: 33);
(TCTA)11 (TCTG)5 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)13 TCGTCT (SEQ ID NO: 34); or
(TCTA)13 (TCTG)5 (TCTA)3 TA (TCTA)3 TCA (TCTA)2 TCCATA (TCTA)12 TCGTCT (SEQ ID NO: 35); or at least 75% homologous thereto;
vi) an allelic ladder for locus D18S51 comprising an allele comprising or consisting of sequence:
(AGAA)8 (SEQ ID NO: 36); or at least 75% homologous thereto.
Preferably the mixture includes allelic ladders for a plurality of loci. It is particularly preferred that the mixture include allelic ladders for at least four loci. Preferably the mixture includes allelic ladders for a plurality of loci selected from HUMVWFA31/A, HUMTHO1, D8S1179, HUMFIBRA/FGA, D21S11 and D18S51. Preferably the mixture includes allelic ladders for at least four of these loci. In its most preferred form the mixture includes allelic ladders for all of these loci.
Preferably the mixture includes an amelogenin sex test.
Preferably one or more of the allelic ladders in the mixture includes at least 7 alleles and more preferably at least 12 alleles. Preferably a plurality, and particularly all, of the allelic ladders of the mixture include at least 8 and more preferably at least 10 alleles.
Preferably one or more or all of the ladders, if present in the mixture, may be provided such that: the HUMVWFA31/A allelic ladder includes at least 9, more preferably 11 and ideally 12 alleles; the HUMTHOl allelic ladder includes at least 7, more preferably 9 and ideally 10 alleles; the D8S1179 allelic ladder includes at least 9, more preferably 12 and ideally 13 alleles; the HUMFIBRA/FGA allelic ladder includes at least 18, more preferably 26 and ideally 28 alleles or is present as HUMFIBRA/FGA/LW and HUMFIBRA/FGA/HW with the HUMFIBRA/FGA/LW ladder including at least 16 more preferably 18 and ideally 20 alleles, the HUMFIBRA/FGA/HW ladder including at least 6, more preferably at leats 7 and ideally 8 alleles; the D21S11 allelic ladder includes at least 14, more preferably 16 and ideally 17 alleles; and the D18S51 ladder includes at least 15, more preferably 19 and ideally 20 alleles.
Preferably one or more of the allelic ladders in the mixture comprises at least 4 pairs of alleles 4 base pairs from each other. More preferably at least 10 pairs, and ideally at least 12 pairs of alleles are so provided. Preferably one or more or all the allelic ladders, if present in the mixture, may be provided such that: the HUMVWFA31/A allelic ladder includes at least 7, more preferably 10 and ideally 11 pairs of alleles 4 base pairs from each other; the HUMTHO1 allelic ladder includes at least 5, more preferably 6 and ideally 7 pairs of alleles 4 base pairs from each other; the D8S1179 allelic ladder includes at least 8, more preferably 11 and ideally 12 pairs of alleles 4 base pairs from each other; the HUMFIBRA/FGA allelic ladder includes at least 17, more preferably 20 and ideally 23 pairs of alleles 4 base pairs from each other; the D21S11 allelic ladder includes at least 3 and ideally 4 pairs of alleles 4 base pairs from each other; and the D18S51 ladder includes at least 13, more preferably 18 and ideally 19 pairs of alleles 4 base pairs from each other. The D21S11 allelic ladder may, or may further include, at least 8, more preferably 11 and ideally 12 pairs of alleles 8 base pairs from each other.
Preferably the allele sequences have at least 85% homogeneity with the listed sequences. More preferable levels of even 90% or at least 95% may be provided. Ideally the exact sequences listed are included within the alleles. In their most preferred form the alleles consist of the listed sequences.
The alleles may further include flanking sequences, i.e., between the primer and STR.
Preferably the HUMVWFA31/A ladder includes alleles ranging from 130, more preferably 126 and ideally 122 base pairs upwards and/or from 166 base pairs downwards. Preferably the HUMTHO1 ladder includes alleles ranging from 150 base pairs upwards and/or 189 base pairs downwards. Preferably the D8S1179 ladder includes alleles ranging from 157 base pairs upwards and/or 201, and more preferably 205 base pairs downwards. Preferably the HUMFIBRA/FGA ladder includes alleles ranging from 173 base pairs upwards and/or 298, more preferably 302 and ideally 310 base pairs downwards. Preferably the D21S11 ladder includes alleles ranging from 203 base pairs upwards and/or 255 or more preferably 259 base pairs downwards. Preferably the D18S51 ladder includes alleles ranging from 270 or more preferably 266 base pairs upwards and/or 326 or 330 or 334 or 338 or even 342 downwards.
According to a second aspect of the invention we provide an allelic ladder mixture comprising an allelic ladder for one or more of the following loci, with lowest molecular weight allele and/or uppermost molecular weight allele as follows:
Preferably one or more of the loci ladders have both the upper and lower limits specified. Preferably all the loci ladders have the full ranges listed.
Preferably the mixture includes allelic ladders for a plurality of loci. It is particularly preferred that the mixture include allelic ladders for at least four loci. Preferably the mixture includes allelic ladders for a plurality of loci selected from HUMVWFA31/A, HUMTHO1, D8S1179, HUMFIBRA/FGA, D21S11 and D18S51. Preferably the mixture includes allelic ladders for at least four of these loci. In its most preferred form the mixture includes allelic ladders for all of these loci.
The intervals of alleles in the ladders and/or number of alleles in the ladders may be as specified in the first aspect of the invention. This aspect may include any of the other features specified elsewhere in the application.
The ladder mixtures of the first and/or second aspect of the invention may further include one or more of PARR buffer, primer(s), or Taq polymerase.
According to a third aspect of the invention we provide a method of analysing one or more samples comprising :
a) obtaining genomic DNA from the sample;
b) amplifying the DNA;
c) obtaining an indication of one or more of the constituent parts of the sample; and comparing the indications with an allelic ladder mixture comprising one or more of the following allelic ladders:
i) an allelic ladder for locus HUMVWFA31/A comprising one or more of alleles comprising or consisting of sequences:
ii) an allelic ladder for locus HUMTHO1 comprising or consisting of sequence:
iii) an allelic ladder for locus D8S1179 comprising one or more of alleles comprising or consisting of sequences:
iv) an allelic ladder for locus HUMFIBRA/FGA comprising one or more of alleles comprising or consisting of the sequences:
v) an allelic ladder for locus D21S11 comprising one or more of alleles comprising or consisting of sequences:
vi) an allelic ladder for locus D18S51 comprising an allele comprising or consisting of sequence:
including allelic ladders or alleles 75% homologous thereto.
The allelic ladder mixture may possess other features specified in the first or second aspects of the invention or elsewhere in this application.
Preferably the DNA sample is one or more of a sample taken from the scene of a crime, a sample associated with the scene of a crime, a sample obtained from a suspect, a sample obtained from a human under consideration (for instance for paternity or maternity analysis) or a reference sample. The sample may be in the form of blood, hair, skin or bodily fluid.
Preferably the sample is amplified using a polymerase chain reaction. Preferably primers for one or more of loci HUMVWFA31/A, HUMTHOl, D8S1179, HUMFIBRA/FGA, D21S11 or D18S51 are employed. The primers may be dye or otherwise labelled.
According to a fourth aspect of the invention we provide one or more alleles comprising or consisting of sequences:
or at least 75% homologous thereto.
Preferably the alleles are provided purified from alleles other than those of HUMVWFA31/A, HUMTHO1, D8S1179, HUMFIBRA/FGA, D21511, D18551 or AMG loci.
According to a fifth aspect of the invention we provide the use of an allelic ladder according to the first aspect of the invention and/or an allele according to the fourth aspect of the invention for comparison with a DNA analysis result.
The analysis may be a DNA profile of a sample. The profile may be based on analysis of one or more loci, in particular including one or more of HUMVWFA31/A, HUMTHO1, D8S1179, HUMFIBRA/FGA, D21S11, D18S51 or AMG. The sample may be from the scene of a crime, associated with the scene of a crime or comprise a bodily fluid sample. The sample may be used to compare two or more individuals, or samples arising therefrom, for instance in paternity and/or maternity analysis.
According to a sixth aspect of the invention we provide a method of producing an allelic ladder or mixture thereof by subjecting the ladders of the first, second or fourth aspects of the invention to PCR.
The invention will now be described, by way of example only, and with reference to the accompanying figure in which:
a and 1b illustrates the locus, allele designation and size for an embodiment of the invention;
a shows an electrophoretogram of the allelic ladder for Amelogenin (AMG);
b shows an electrophoretogram of the allelic ladder for HUMVWFA31/A;
c shows an electrophoretogram of the allelic ladder for HUMTHO1;
d shows an electrophoretogram of the allelic ladder for D8S1179;
e shows an electrophoretogram of the allelic ladder for HUMFIBRA, low and high molecular weights;
f shows an electrophoretogram of the allelic ladder for D21S11;
g shows an electrophoretogram of the allelic ladder for D18S51;
a shows the sequence of selected alleles forming the HUMVWFA31/A ladder (SEQ ID NOS 1-2 and 39, respectively, in order of appearance);
b shows the sequence of selected alleles forming the HUMTHO1 ladder (SEQ ID NO: 4);
c shows the sequence of selected alleles forming the D8S1179 ladder (SEQ ID NOS 5-6, respectively, in order of appearance);
d shows the sequence of selected alleles forming the HUMFIBRA ladder (SEQ ID NOS 7-18, respectively, in order of appearance);
e shows the sequence of selected alleles forming the D21S11 ladder (SEQ ID NOS 19-35, respectively, in order of appearance); and
f shows the sequence of selected alleles forming the D18S51 ladder (SEQ ID NO: 36).
An allelic ladder mixture illustrative of the present invention is provided for loci HUMTHO1, D21S11, D8S1179, HUMVWFA31/A, HUMFIBRA/FGA and amelogenin sex test. The loci nomenclature is standard, corresponding to that used in the GENEBANK database.
The ladder mixture includes a significant number of alleles for each locus so as to provide a base line for comparison across a wide range. The loci, allelic designation and base pair sizes for the mixture are shown in
The allelic ladder mixture was presented in PARR buffer (containing Tris and 1.5 mM Mg ions at pH8.0) obtained from Cambio, primers obtained from Oswell and Taq polymerase from Perkin Elmer.
Electrophoretograms for the allelic ladders are shown in
a to 3f show the sequences for the alleles identified in
The allelic ladder mixture discussed above was produced according to the following techniques. Buccal swabs and/or bloodstains were used as the sample sources. The genomic DNA was extracted using the chelex procedure described by Walsh et al. 1991 Bio. Techniques 1 91-98.
The recovered DNA was quantified by dot hybridisation using a higher primate specific probe, as disclosed in Walsh et al. 1992 Nucleic Acids Res. 20 5061-5065.
Each sample was then amplified according to the conditions set out below in Table 1 with unlabelled oligonucleotide primers, the sequences for which are disclosed in Urquhart et al. 1995 Bio Techniques 18 116-121 and Oldroyd et al. 1995 Electrophoresis 16 334-337.
Individual alleles were then isolated and sequence analysis was carried out according to the methods of Barber et al. 1996 Int. Journal Leg. Med. 108 180-185 and Barber and Parkin 1996 Int. Journal Leg. Med. 109 62-65. Both DNA strands of each allele reported were sequenced and the sequences provided in
The illustrations of the alleles provided in
To prepare the ladder cocktail amplification of the alleles is necessary. This process was performed by amplifying the purified single alleles described above using a labelled primer in each case. For the locus HUMFIBRA/FGA the ladder was produced from two separate mixes, discussed in more detail below. The primers used are disclosed in Urquhart et al. 1995 Bio Techniques 18 116-121 and Oldroyd et al. 1995 Electrophoresis 16 334-337 and were employed according to the conditions set out above in Table 1.
The singleplexs produced in this way were analysed on an Applied Bio systems 377 automated sequencer to confirm the sequences. The sequences obtained from the profiling system are one base longer than those determined form the DNA sequencing technique initially discussed above. This is due to the ability of DNA polymerase from Thermus aquaticus to catalyse a non-template mediated addition of a deoxyribonucleotide to the 3′ hydroxyl of PCR products. This is generally known as the “n+1” product and can be generated in preference to the “n” product. The results reported here, however, refer to the “n” product rather than the “n+1” product for which the labelled primer PCR conditions have been optimised to produce.
The products of the amplification process for each locus were then diluted, mixed with one another and reanalysed to produce a single ladder for each loci having even peak heights. An initial level of 1000 Arbitary Units, AU, was increased to 1000-5000 AU to give greater signal strength and volume for the ladder.
The single ladders produced in this way were then mixed together to give the cocktail discussed above. The proportions of each ladder used are controlled to give balanced peak areas. The cocktail was then validated using Applied Biosystems 373A and Applied Biosystems 377 automated sequencers with Genescan and Genotyper software.
Allelic ladders according to the invention can be prepared by applying PCR amplification techniques to a pre-existing sample of the allelic ladder mixture. Alternatively the allelic ladders can be constructed from the sequence information provided herein.
The new ladders disclosed above significantly extends the range of alleles which can be identified in any DNA profiling system.
The allelic ladder mixture is used as a control sample alongside samples from known or unknown individuals which are then segregated according to size in a gel. Alleles in the sample under test can be designated by the known alleles in the control if they are within 0.5 bases of one another. Alleles falling outside this range are estimated based on their position relative to the ladder.
Using the standard nomenclature discussed above, the ladder range for each locus, defined by the extreme low molecular weight and extreme high molecular weight alleles are:
The allelic ladders also enable the identification of certain rare and hence highly discriminatory alleles in DNA profiling, thus increasing the profiling systems power.
For the various locus certain alleles are of particular significance as follows:
The primers used for this locus were labelled with 6-FAM. The polymorphic region of this locus is based around a tetranucleotide motif repeat, (TCAT)n, where n=4 to 13. Particular alleles provided by the present invention include 4, 9.3, 10 and 13.3. The 9.3 and 13.3 alleles were found to have a deletion of a thiamine nucleotide at either the last base of the 4th repeat unit or the first base of the 5th repeat unit. The 13.3 allele notably possesses a non-consensus tetranucleotide (TCGT) at the 13th repeat.
The primers for this locus were also labelled with 6-FAM. The allele range extends from 53 to 81 and significantly includes alleles 53, 56, 57, 79 and 81. The polymorphic region of the D21S11 alleles is relatively complex in structure and is based around the tetranucleotide TCTR, where R is A or G (following the ambiguity codes of the Nomenclature Committee of the International Union of Biochemistry), as well as containing invariant hexa-, tri- and di-nucleotides. Both allele 54 and allele 56 deviate from this general structure in that they possess a deletion of a 14 base pair TA(TCTA)3 (SEQ ID NO: 37) unit immediately prior to the invariant TCA tetranucleotide.
Again primers with a 6-FAM label were used. The ladder extends to 20 distinct alleles with particularly significant alleles at 8, 9, 23, 24, 25, 26 and 27. The polymorphic region is based around a simple tetranucleotide repeat motif (AGAA)n (SEQ ID NO: 38), where n is 8 to 27.
The primers used for this locus were labelled with TET. The ladder extends from alleles 7 to 19, based on 13 separate alleles. Significant alleles include 7, 15, 18 and 19. Different generalised structures were observed between the upper and lower molecular weight ends of the ladder. In the lower molecular weight area, 161 to 177 base pairs, a simple repeat region based on the tetranucleotide TCTA exists. In the higher weight region, 181 to 201 base pairs, a compound repeat region composed of the tetranucleotide TCTR was found.
HEX labelled primers were used for this locus. The ladder covers alleles between 10 and 21, based on 12 alleles in total. Noteworthy alleles 10, 11 and 12 are included. The polymorphic unit is generally composed of a compound repeat following the pattern (TCTR)n. For the 13 and 14 alleles a non-consensus TCCA tetranucleotide at the 10th and 11th repeats was found.
This locus also employed HEX labelled primers. As mentioned above this ladder was constructed in two separate components. A low molecular weight and high molecular weight mix was used to produce the overall ladder. The low molecular weight mix ranges from allele 16.1 to 34.2 and the high molecular weight mix from allele 42.2 to 50.2.
The low MW mix includes significant alleles 16.1, 28, 30, 30.2, 31.2, 32.2, 33.2 and 34.2. The high MW mix includes noteworthy alleles 42.2, 43.2, 44.2, 45.2, 47.2, 48.2 and 50.2.
In general the HUMFIBRA/FGA alleles have a polymorphic unit based around the compound repeat YYBY, with the alleles in the upper part of the weight range being more complex in structure than those in the lower part. Within the general framework, allele 16.1 has a T nucleotide addition in the repeat region and allele 27 has a C to T transition in the 19th repeat unit (CTTT to CCTT). The upper MW allele range includes a stutter peak which is 4 base pairs smaller than the 50.2 allele. This artifact corresponds to allele 49.2 which has not currently been determined.
Primers for this locus were once again labelled with 6-FAM. The sequence data revealed an X specific product of 105 base pairs and a Y specific product of 111 base pairs.
HUMTHO1 allele sequences
D21S11 alleles sequences
D18S51 allele sequences
D8S1179 allele sequences
HUMVWAF31/A allele sequences
(Note also that the allele has an atypical 3′ flanking sequence. The usual sequence is TCCA TCTA T. In this allele the sequence is (TCCA)2T.
HUMFIBRA(FGA) allele sequences
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The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.
| Number | Date | Country | Kind |
|---|---|---|---|
| 9713597.4 | Jun 1997 | GB | national |
This application is a coninutation of U.S. patent application Ser. No. 12/632,608, filed Dec. 7, 2009, which is a conintuation of U.S. patent application Ser. No. 11/821,259, filed Jun. 21, 2007, now U.S. Pat. No. 7,645,580, which is a continuation of U.S. patent application Ser. No. 11/244,331, filed Oct. 4, 2005 (abandoned), which is a continuation of U.S. patent application Ser. No. 09/910,183, filed Jul. 20, 2001, now U.S. Pat. No. 7,087,380, which is a continuation of U.S. patent application Ser. No. 09/706,525, filed Nov. 3, 2000 (abandoned), which is a continuation of U.S. patent application Ser. No. 09/498,567, filed Feb. 4, 2000 (abandoned), which is a continuation of U.S. patent application Ser. No. 09/107,029, filed Jun. 29, 1998 (abandoned), which claims priority to United Kingdom Application No. 9713597.4, filed Jun. 28, 1997, which for purposes of disclosure are incorporated herein by specific reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12632608 | Dec 2009 | US |
| Child | 13089099 | US | |
| Parent | 11821259 | Jun 2007 | US |
| Child | 12632608 | US | |
| Parent | 11244331 | Oct 2005 | US |
| Child | 11821259 | US | |
| Parent | 09910183 | Jul 2001 | US |
| Child | 11244331 | US | |
| Parent | 09706525 | Nov 2000 | US |
| Child | 09910183 | US | |
| Parent | 09498567 | Feb 2000 | US |
| Child | 09706525 | US | |
| Parent | 09107029 | Jun 1998 | US |
| Child | 09498567 | US |
