SEQanswers - Threads Tagged with snp

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Threads Tagged with snp

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Threads Tagged with snp
	Thread / Thread Starter	Last Post	Replies	Views	Forum
	Postdoc position and bioinformatician position in cancer genomics aromanel	01-14-2018 06:20 AM by aromanel	0	352	Academic/Non-Profit Jobs
	Help filtering variants from TSV file using text processing programming language MGlenn	12-06-2017 01:20 PM by neavemj	7	664	Bioinformatics
	Webinar on Analysis of Variants using GeneSpring GX 14.9 on 6 Dec 2017 Strandlife	11-27-2017 12:31 AM by Strandlife	1	1,711	Webinar Series
	Validating SNP calls quality jomare1188	09-22-2017 10:07 AM by jomare1188	0	432	Bioinformatics
	Decoding the landscape of RNA modifications from transcriptome sequencing data yjhua2110	09-05-2017 04:17 PM by yjhua2110	6	3,671	RNA Sequencing
	The landscape of RNA modifications from high-throughput sequencing data rnaNGS	09-01-2017 02:17 AM by rnaNGS	5	2,211	Bioinformatics
	RNA Modification Database and The Map of RNA Modifications rnaNGS	08-21-2017 04:53 AM by rnaNGS	0	719	RNA Sequencing
	how to extract gene name for non-synonymous SNPs from annotated vcf file for GO analy R.66	07-21-2017 02:34 AM by R.66	0	397	Bioinformatics
	how to extract gene name for non-synonymous SNPs from annotated vcf file for GO analy rezakhalkhali	07-21-2017 01:56 AM by rezakhalkhali	0	433	Bioinformatics
	Research Officer - Systems Genomics mbrozynska	06-27-2017 02:18 PM by mbrozynska	0	304	Academic/Non-Profit Jobs
	Calling variants when mapping reads from different species than reference gruberjd	05-19-2017 11:52 AM by Brian Bushnell	3	1,268	Genomic Resequencing
	How to generate VCF from HISAT2 pre-built SNP index? jol.espinoz	04-30-2017 11:03 AM by jol.espinoz	0	1,039	Genomic Resequencing
	Remove SNP in segment duplication and repeat region cindylanzao	04-27-2017 05:47 PM by cindylanzao	4	760	Bioinformatics
	Meaning of the P-value relating to SNP (single nucleotide polymorphism) nhaus	03-08-2017 03:40 AM by mastal	5	935	Bioinformatics
	Imterpretting BAYENV2 sells78	02-18-2017 09:58 AM by sells78	0	764	Bioinformatics
	Aligning Reads with Overhangs on the Ends (Edges) of Reference Contigs or Scaffolds Fatih	12-01-2016 03:23 AM by Fatih	0	736	Bioinformatics
	epiGBS Niels Wagemaker	10-27-2016 03:45 AM by Niels Wagemaker	2	1,911	Epigenetics
	Illumina vs. Agilent Exome enrichment - higher false positive rates markusl	09-22-2016 07:22 AM by Geneus	9	6,118	Genomic Resequencing
	Need help understanding what "b-allele" refers to antifolate	09-21-2016 09:08 PM by antifolate	0	867	Bioinformatics
	HISAT2 tran and snp indices RichardJActon	05-12-2016 02:50 AM by RichardJActon	0	1,275	RNA Sequencing
	Research Technician @ Harbor Branch, Florida Atl Univ HeidiJTP	05-05-2016 08:15 AM by HeidiJTP	0	1,369	Academic/Non-Profit Jobs
	A problem of using Samtools to make VCF file watermelon1037	04-19-2016 08:48 PM by watermelon1037	0	838	Bioinformatics
	How to get SNP abundance from a metagenomic VCF? thh32	01-15-2016 07:16 AM by thh32	0	933	Bioinformatics
	Snp discovery without a reference ( 1 2) lletourn	01-12-2016 05:15 AM by arthurmelo	38	12,783	De novo discovery
	Big question - Transcriptome annotation Dampor	01-02-2016 03:25 AM by kurban910	7	2,746	Bioinformatics
	call indel and SNP by varscan doublealice	12-03-2015 08:32 AM by Jane M	1	1,432	Bioinformatics
	Non-random Illumina sequencing error? HMorrison	11-12-2015 01:03 PM by blancha	2	1,188	Illumina/Solexa
	Strange VAF distribution across SNP positions in WGS sample graubner277	10-26-2015 05:08 AM by graubner277	2	963	Bioinformatics
	Strange Fst distribution in BayeScan sacketlc	10-06-2015 09:35 AM by GenoMax	1	1,253	Bioinformatics
	error unable to parse known snp litali	10-06-2015 04:00 AM by litali	0	757	Bioinformatics

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