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點(diǎn)擊查看下載法庭科學(xué)DNA研究方案 Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing相關(guān)資料，進(jìn)一步了解產(chǎn)品。

IF: 1.276  相關(guān)產(chǎn)品：Microreader? 19X ID System

6. IF: 5.637  相關(guān)產(chǎn)品：Microreader? 23sp ID System 

Genetic polymorphisms of 22 autosomal STR loci in Chinese Han population.  Forensic Science International: Genetics Supplement Series, 2015. 

7. IF: 5.206  相關(guān)產(chǎn)品：Microreader? 20A ID System

Thalassaemia intermedia caused by coinheritance of a β‐thalassaemia mutation and a de novo duplication of α‐globin genes in the paternal allele. BRIT J HAEMATOL, 2019. 

8. IF: 4.884  相關(guān)產(chǎn)品：Microreader? 21 (Direct) ID System

Developmental Validation of Y-SNP Pedigree Tagging System: a panel via quick ARMS PCR. FORENSIC SCI INT-GEN, 2020.

9. IF: 3.439  相關(guān)產(chǎn)品：Microreader? 21 (Direct) ID System

Patient-derived xenografts of different grade gliomas retain the heterogeneous histological and genetic features of human gliomas. CANCER CELL INT, 2020.

10. IF: 2.569  相關(guān)產(chǎn)品：Microreader? 20A ID System

Developmental validation of the MicroreaderTM 20A ID system. Electrophoresis, 2019. 

11. IF: 2.4 

Development one novel multiplex PCR system for forensic individual identification using insertion/deletion polymorphisms. ELECTROPHORESIS, 2019.

12. IF: 2.094  相關(guān)產(chǎn)品：Microreader? 19X ID System

Genetic characterization of 19 X-STRs in Sierra Leone population from Freetown. INT J LEGAL MED, 2020.

13. IF: 2.094  相關(guān)產(chǎn)品：Microreader? 24Y ID System

Developmental validation study of a 24-plex Y-STR direct amplification system for forensic application. INT J LEGAL MED, 2019.

14. IF: 1.99  相關(guān)產(chǎn)品：Microreader? 21 (Direct) ID System

Genetic and chromosomal variation-caused inconsistencies in two parental tests. FORENSIC SCI INT, 2019.

15. IF: 1.276  相關(guān)產(chǎn)品：Microreader? 19X ID System

Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing. Legal Medicine, 2017. 

閱微基因擁有一代測(cè)序、二代測(cè)序、qPCR 及基因芯片等平臺(tái)，可以多方位對(duì)人源細(xì)胞、微生物等的STR、SNP、DNA 甲基化、Mt-DNA 進(jìn)行單一 / 集成化的長(zhǎng)度多態(tài)性或序列多態(tài)性等方面檢測(cè)，獲取從簡(jiǎn)單到復(fù)雜的遺傳信息，為法醫(yī)的研究提供更多的解決方案及簡(jiǎn)易的工作流程。

重要合作成果

1. Genetic distribution of 39 STR loci in 1027 unrelated Han individuals from Northern China. FSI: Genetics（影響因子：5.637）

2. Concurrent copy number variations on chromosome 8 and 22 combined with mutation at FGA locus revealed in a parentage testing case.FSI: Genetics（影響因子：5.637）

3. Genetic polymorphism of 22 autosomal STR markers in a Han population of Southern China. FSI: Genetics（影響因子：5.637）

4. Validation of the Microreader 23sp ID system: A new STR 23-plex system for forensic application. FSI: Genetics（影響因子：5.637）

5.A genomic audit of newly-adopted autosomal STRs for forensic identification. FSI: Genetics（影響因子：5.637）

6. Development of a rapid 21‐plex autosomal STR typing system for forensic applications. Electrophoresis(影響因子：2.569)

7. Inconsistent genotyping call at DYS389 locus and implications for interpretation. International Journal of Legal Medicine(影響因子：2.316)

8. Population data for 22 autosomal STR loci in the Uygur ethnic minority. International Journal of Legal Medicine(影響因子：2.316)

9. Forensic molecular genetic diversity analysis of Chinese Hui ethnic group based on a novel STR panel. International Journal of Legal Medicine(影響因子：2.316)

法庭科學(xué)DNA研究方案

閱微基因擁有一代測(cè)序、二代測(cè)序、qPCR 及基因芯片等平臺(tái)，可以多方位對(duì)人源細(xì)胞、微生物等的STR、SNP、DNA 甲基化、Mt-DNA 進(jìn)行單一 / 集成化的長(zhǎng)度多態(tài)性或序列多態(tài)性等方面檢測(cè)，獲取從簡(jiǎn)單到復(fù)雜的遺傳信息，為法醫(yī)的研究提供更多的解決方案及簡(jiǎn)易的工作流程。

重要合作成果

1. IF: 6.513  相關(guān)產(chǎn)品：Microreader? 21 (Direct) ID System

Investigation of cross-contamination among human cell lines used in China. International journal of cancer, 2017. 

2. IF: 5.637  相關(guān)產(chǎn)品：Microreader? 23sp ID System 

Analysis of genetic polymorphisms and mutations at 23 autosomal STR loci in Guangdong Han population. Forensic Science International: Genetics, 2019. 

3. IF: 5.637  相關(guān)產(chǎn)品：Microreader? 23sp ID System 

Validation of the Microreader? 23sp ID system: A new STR 23-plex system for forensic application.  Forensic Science International: Genetics, 2017. 

4. IF:5.637  相關(guān)產(chǎn)品：Microreader? 23sp ID System 

Multistep microsatellite mutation at D18S51 locus in a parentage testing case. Forensic Science International: Genetics Supplement Series, 2017. 

5. IF: 5.637  相關(guān)產(chǎn)品：Microreader? 23sp ID System 

Genetic polymorphism of 22 autosomal STR markers in a Han population of Southern China.  Forensic Science International: Genetics, 2016.  

法庭科學(xué)DNA研究方案 Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing,法庭科學(xué)DNA研究方案

法庭科學(xué)DNA研究方案 Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing信息由北京閱微基因技術(shù)有限公司為您提供，如您想了解更多關(guān)于法庭科學(xué)DNA研究方案 Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing報(bào)價(jià)、型號(hào)、參數(shù)等信息，歡迎來(lái)電或留言咨詢。

注：該產(chǎn)品未在中華人民共和國(guó)食品藥品監(jiān)督管理部門申請(qǐng)醫(yī)療器械注冊(cè)和備案，不可用于臨床診斷或治療等相關(guān)用途