현재 (구)Biomedical Genomics Workbench는 CLC Genomics Workbench의 플러그인으로 들어가게 되었습니다.

CLC Genomics Workbench에서 Biomedical Genomics Analysis 라는 플러그인을 이용하여 분석하는 것이 (구)Biomedical Genomics Workbench와 동일 혹은 더 나은 기능을 가지고 있다고 보시면 됩니다.

이전에 (구)Biomedical Genomics Workbench로 publish 된 논문 목록은 아래와 같습니다.

1. New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy.
   Hum. Mol. Genet. 2017 Aug 01;26(15):2923-2932. PMID: 28472301. Pinggera A, Mackenroth L, Rump A, Schallner J, Beleggia F, Wollnik B, Striessnig J
    
2. Isolated congenital hepatic fibrosis associated with TMEM67 mutations: report of a new genotype-phenotype relationship.
   Clin Case Rep 2017 Jul 01;5(7):1098-1102. PMID: 28680603. Vogel I, Ott P, Lildballe D, Hamilton-Dutoit S, Vilstrup H, Grønbæk H
    
3. HOXA7, HOXA9, and HOXA10 are differentially expressed in clival and sacral chordomas.
   Sci Rep 2017 May 17;7(1):2032. PMID: 28515451. Jäger D, Barth TFE, Brüderlein S, Scheuerle A, Rinner B, von Witzleben A, Lechel A, Meyer P, Mayer-Steinacker R, Baer AV, Schultheiss M, Wirtz CR, Mölle… More

4. Identification of potential immune targets in controlling Endometrioid Endometrial Carcinoma metastatic progression.
   The Journal of Immunology. _. Jean-Noel Billaud, Stuart Tugendreich and Debra Toburen.

5. A SNP panel for identity and kinship testing using massive parallel sequencing.
   Int. J. Legal Med. 2016 Jul 01;130(4):905-14. PMID: 26932869. Grandell I, Samara R, Tillmar AO

 

CLC Genomics Workbench를 이용하여 publish 된 논문은 수천편이 되고, 아래 링크를 통해 검색하시면 해당 논문들 목록을 확인하실 수 있습니다.

>>>CLC Genomics Workbench publications