287 skills found · Page 1 of 10
xavier-zy / Awesome Pytorch List CNVersionAwesome-pytorch-list 翻译工作进行中......
YDHCUI / CNVD 2020 10487 Tomcat Ajp LfiTomcat-Ajp协议文件读取漏洞
broadinstitute / InfercnvInferring CNV from Single-Cell RNA-Seq
etal / CnvkitCopy number variant detection from targeted DNA sequencing
00theway / Ghostcat CNVD 2020 10487Ghostcat read file/code execute,CNVD-2020-10487(CVE-2020-1938)
cnpack / CnvclCnPack VCL Components
bkfish / CNVD 2020 10487 Tomcat Ajp Lfi ScannerCnvd-2020-10487 / cve-2020-1938, scanner tool
lgmgeo / AnnotSVAnnotation and Ranking of Structural Variation
jas502n / CNVD C 2019 48814WebLogic wls9-async反序列化远程命令执行漏洞
abyzovlab / CNVnatora tool for CNV discovery and genotyping from depth-of-coverage by mapped reads
abyzovlab / CNVpytora python extension of CNVnator -- a tool for CNV analysis from depth-of-coverage by mapped reads
ttonys / Scrapy CVE CNVD漏洞监控，基于scrapy，scrapy-redis，获取每日最新的CVE和CNVD漏洞，邮件通知
Ryze-T / CNVD 2022 10270 LPE基于向日葵RCE的本地权限提升，无需指定端口
kharchenkolab / NumbatHaplotype-aware CNV analysis from single-cell RNA-seq, ATAC-seq, and multiome
RaiderZP / Cnvd Fofa Gather（由于fofa接口改变，所以该脚本已经失效了哦）通过公司名称，在fofa上搜索可能存在通用产品的公司；如果想挖掘cnvd证书，可导出注册资金大于5000w的公司到这个脚本中进行通用系统收集。
icbi-lab / InfercnvpyInfer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
dkoboldt / VarscanVariant calling and somatic mutation/CNV detection for next-generation sequencing data
ShixiangWang / Sigminer🌲 An easy-to-use and scalable toolkit for genomic alteration signature (a.k.a. mutational signature) analysis and visualization in R https://shixiangwang.github.io/sigminer/reference/index.html
Illumina / CanvasCanvas - Copy number variant (CNV) calling from DNA sequencing data
7kbstorm / WebLogic CNVD C2019 48814WebLogic CNVD-C-2019_48814 CVE-2017-10271 Scan By 7kbstorm
