Clc Main Workbench Crack Mac
차례. CLC Genomics Workbench는 최근 Next Generation Sequencing 기술의 발달로 기존보다 수십 배, 수백 배 많이 생산되고 있는 NGS 데이터를 분석할 수 있는 데스크탑용 소프트웨어입니다. 기존의 sequencing 데이터 뿐만 아니라 다양한 NGS 포맷(Roche, Illumina, Ion torrent, Helicos data)의 분석을 지원하며, SIMD 기술의 적용으로 막대한 양의 NGS 시퀀싱 데이터를 고속으로 분석하고 scaffolding 기능이 새롭게 탑재되어 연구자에게 최상의 분석결과를 제시합니다. 또한 RNA-seq, ChIP-seq 분석 툴이 추가되어 Genomics, Transcriptomics, Epigenomics 분야까지도 응용 가능합니다. 그 밖에 Main Workbench(DNA, RNA, Protein 통합 분석 툴)의 기능을 모두 포함하고, Genomics gateway 같은 최신의 분석 기법들을 Plug-In 모듈로 제공함으로써 다양한 생물 정보 분석을 편리하게 수행할 수 있습니다. Main Features.
Assembly Primer design Molecular cloning SNP detection Multiple alignment Digital gene expression RNA structure prediction Pattern search Blast search Application Note Cancer Genomics. Plant & Animal Genomics. Medical genomics. Microbial & Metagenomics. System Requirement. Windows Vista, Windows 7, Windows 8, Windows 10 or Windows Server 2008. Mac OS X 10.7 or later.
Linux: RHEL 5.0 or later. SUSE 10.2 or later. Fedora 6 or later. Minimum linux versions needed for the SRA download functionality: Red Hat 6, Fedora 12, and SUSE 11. 64 bit operating system. 2 GB RAM required. 4 GB RAM recommended.
1024 x 768 display required. 1600 x 1200 display recommended. Intel or AMD CPU required Special requirements for the 3D Molecule Viewer. A graphics card capable of supporting OpenGL 2.0.
Updated graphics drivers. Please make sure the latest driver for the graphics card is installed. A discrete graphics card from either Nvidia or AMD/ATI. Modern integrated graphics cards (such as the Intel HD Graphics series) may also be used, but these are usually slower than the discrete cards. Indirect rendering (such as x11 forwarding through ssh), remote desktop connection/VNC, and running in virtual machines is not supported. Special requirements for read mapping.
E. Coli K12 ( 4.6 megabases).
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Minimum: 2Gb RAM. Recommended: 4Gb RAM. C.
Commercial tools. Strand NGS. offers many different tools including alignment, RNA-Seq, DNA-Seq, ChIP-Seq, Small RNA-Seq, Genome Browser, visualizations, Biological Interpretation, etc.
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Supports workflows “one can import the sample data in FASTA, FASTQ or tag-count format. In addition, prealigned data in SAM, BAM or Illumina-specific ELAND format can be directly imported for analysis.”.
Alignment feature: Supports alignment from Illumina, Ion Torrent, 454 (Roche), and Pac Bio. DNA-Seq Feature, can annotate with dbSNP.
CLC Genomics Workbench. (QIAGEN).