Mike Hann’s Post

Join us for an exciting webinar that will provide considerations for designing copy number analysis experiments and tips for deciding on the best analysis platform! Traditional copy number variation (CNV) is defined as a modification in the genome where the number of copies of a genomic DNA sequence differs from a reference or standard. Genomic alterations such as insertions, deletions, inversions, or translocation can lead to biallelic or multiallelic CNVs. CNVs are linked to susceptibility or resistance to disease, and thus are a critical area for detailed study. Other copy number analysis includes somatic copy number changes and gene transfer research. Register today at https://lnkd.in/drkQ6Yt6 #thermofisheremp

The Target to Patient T2P 2024 conference at Wellcome Genome Campus on April 29/30 is now open for registration with great early bird discounts and a fantastic line up of speakers (full list is here https://lnkd.in/eFmPy-hJ)   https://lnkd.in/eVRk2nyF Emanuela Cuomo - thank you for agreeing to speak at this exciting conference. We are looking forward to hearing your perspective on how AZ our approaching "intractable" targets with new modalities.   #drugdiscovery #drugdevelopment #organonachip #drugdesign #medicinalchemistry #pharmaceuticalindustry #molecularglue #protac #functionalgenomics #targetvalidation #astrazeneca   From <https://lnkd.in/e4N_sNbr> 

Join us for an exciting webinar that will provide considerations for designing copy number analysis experiments and tips for deciding on the best analysis platform! Traditional copy number variation (CNV) is defined as a modification in the genome where the number of copies of a genomic DNA sequence differs from a reference or standard. Genomic alterations such as insertions, deletions, inversions, or translocation can lead to biallelic or multiallelic CNVs. CNVs are linked to susceptibility or resistance to disease, and thus are a critical area for detailed study. Other copy number analysis includes somatic copy number changes and gene transfer research. Register today at https://lnkd.in/djhkgwDy #thermofisheremp

Join us for an exciting webinar that will provide considerations for designing copy number analysis experiments and tips for deciding on the best analysis platform! Traditional copy number variation (CNV) is defined as a modification in the genome where the number of copies of a genomic DNA sequence differs from a reference or standard. Genomic alterations such as insertions, deletions, inversions, or translocation can lead to biallelic or multiallelic CNVs. CNVs are linked to susceptibility or resistance to disease, and thus are a critical area for detailed study. Other copy number analysis includes somatic copy number changes and gene transfer research. Register today at https://lnkd.in/e743eJwh #thermofisheremp

Join us for an exciting webinar that will provide considerations for designing copy number analysis experiments and tips for deciding on the best analysis platform! Traditional copy number variation (CNV) is defined as a modification in the genome where the number of copies of a genomic DNA sequence differs from a reference or standard. Genomic alterations such as insertions, deletions, inversions, or translocation can lead to biallelic or multiallelic CNVs. CNVs are linked to susceptibility or resistance to disease, and thus are a critical area for detailed study. Other copy number analysis includes somatic copy number changes and gene transfer research. Register today at https://lnkd.in/dbizQekE #thermofisheremp

Join us for an exciting webinar that will provide considerations for designing copy number analysis experiments and tips for deciding on the best analysis platform! Traditional copy number variation (CNV) is defined as a modification in the genome where the number of copies of a genomic DNA sequence differs from a reference or standard. Genomic alterations such as insertions, deletions, inversions, or translocation can lead to biallelic or multiallelic CNVs. CNVs are linked to susceptibility or resistance to disease, and thus are a critical area for detailed study. Other copy number analysis includes somatic copy number changes and gene transfer research. Register today at https://lnkd.in/enZ7Xcbi #thermofisheremp

🚀 Join us for an exciting webinar that will provide considerations for designing copy number analysis experiments and tips for deciding on the best analysis platform!🚀 Traditional copy number variation (CNV) is defined as a modification in the genome where the number of copies of a genomic DNA sequence differs from a reference or standard. Genomic alterations such as insertions, deletions, inversions, or translocation can lead to biallelic or multiallelic CNVs. CNVs are linked to susceptibility or resistance to disease, and thus are a critical area for detailed study. Other copy number analysis includes somatic copy number changes and gene transfer research. Register today at https://lnkd.in/ecic-nz2 #thermofisheremp

Join us for an exciting webinar that will provide considerations for designing copy number analysis experiments and tips for deciding on the best analysis platform! #thermofisheremp Traditional copy number variation (CNV) is defined as a modification in the genome where the number of copies of a genomic DNA sequence differs from a reference or standard. Genomic alterations such as insertions, deletions, inversions, or translocation can lead to biallelic or multiallelic CNVs. CNVs are linked to susceptibility or resistance to disease, and thus are a critical area for detailed study. Other copy number analysis includes somatic copy number changes and gene transfer research. Register today at https://lnkd.in/exkvw_JP #thermofisheremp

Very interesting and timely #immunotoxicology #drugsafety #drugdevelopment article!

More evidence the AI can assist in the development of #raredisease therapies.