I immediately fax you a copy if you give me your number. 翻译结果2复制译文编辑译文朗读译文返回顶部 I fax one of your immediately if you give me your number. 翻译结果3复制译文编辑译文朗读译文返回顶部 I immediately fax you a copy if you give me your number. ...
When you do business, you'll need to identify yourself as a legitimate entity to a variety of stakeholders. One way to do this is to provide an EIN. From opening a bank account to applying for credit to filing your taxes, you'll need an EIN. You can apply for and get an EIN onlin...
Ein Zeiger auf eine IO_STATUS_BLOCK-Struktur, die die endgültige Vervollständigung status und andere Informationen zum Kopiervorgang empfängt. [in] Length Die Länge der zu kopierenden Daten in Bytes. [in] SourceOffset Der Startbyteoffset in der Quelldatei, um den Lesevorgang zu start...
Ein Zeiger auf eine IO_STATUS_BLOCK-Struktur, die die endgültige Vervollständigung status und andere Informationen zum Kopiervorgang empfängt. [in] Length Die Länge der zu kopierenden Daten in Bytes. [in] SourceOffset Der Startbyteoffset in der Quelldatei, um den Lesevorgang zu start...
aIN-MOLD PATTERN (GLOSSY FINISH, PATTERN) IN-MOLD样式 (光滑的结束,样式)[translate] ainvoice in the originals and 1 copy :indicating contract number ,shipping mark,gross and net weight of each package 正在翻译,请等待...[translate]
number, "DestinationBackupVaultArn": "string", "DestinationRecoveryPointArn": "string", "IamRoleArn": "string", "IsParent": boolean, "MessageCategory": "string", "NumberOfChildJobs": number, "ParentJobId": "string", "ResourceArn": "string", "ResourceName": "string", "ResourceType": "...
The contribution of germline copy number variants (CNVs) to risk of developing cancer in individuals with pathogenic BRCA1 or BRCA2 variants remains relatively unknown. We conducted the largest genome-wide analysis of CNVs in 15,342 BRCA1 and 10,740 BRCA
Copy number alterations (CNAs) are among the most important genetic events in cancer, but their detection from sequencing data is challenging because of unknown sample purity, tumor ploidy, and general intra-tumor heterogeneity. Here, we present CNAqc, a
Using a combination of DNA methylation, copy number analysis, whole-exomic sequencing (WES), targeted deep sequencing (TDR) of recurrently mutated CLL driver genes, screening of non-coding mutation and immunogenetic analysis we identified the presence or acquisition of clonal or sub-clonal driver ...
FULL PAPER British Journal of Cancer (2017) 117, 421–431 | doi: 10.1038/bjc.2017.208 Keywords: colon cancer; copy number aberrations; gene expression; stroma; molecular subtypes Comprehensive analysis of copy number aberrations in microsatellite stable colon cancer in view of stromal component M ...