Grch38 Vs Grch37 (updated 2024-11-08)

14 Retrieving missense SNPs of a gene from Ensembl database for human genome assembly GRCh37hg19 [upl. by Leela]

14 Retrieving missense SNPs of a gene from Ensembl database for human genome assembly GRCh37hg19

Duration: 6:12
346 weergaven | 6 jan. 2022

Determining the Human Genome Hg Build of a Dataset Hg18 GRCh37 versus Hg38 GRCh38 [upl. by Alessandro]

Determining the Human Genome Hg Build of a Dataset Hg18 GRCh37 versus Hg38 GRCh38

Duration: 34:29
371 weergaven | 19 okt. 2021

Patches and Haplotypes in the Human Genome [upl. by Ruvolo869]

Patches and Haplotypes in the Human Genome

Duration: 6:10
15,1K weergaven | 21 jun. 2012

What is hg19hg38 All you need to know about human reference genomes Bioinformatics 101 [upl. by Bajaj247]

What is hg19hg38 All you need to know about human reference genomes Bioinformatics 101

Duration: 11:59
6,8K weergaven | 15 jul. 2022

GRCh38 and Ensembl [upl. by Ahsaten679]

GRCh38 and Ensembl

Duration: 27:19
1,5K weergaven | 18 sep. 2014

Genome Builds and NCBI Genome Data Viewer [upl. by Assener]

Genome Builds and NCBI Genome Data Viewer

Duration: 26:10
353 weergaven | 22 mei 2020

Which Human Reference Genome Should You Use hg19 vs hg38 Base Call [upl. by Dragde112]

Which Human Reference Genome Should You Use hg19 vs hg38 Base Call

Duration: 9:30
3K weergaven | 9 jun. 2021

MH Guide lifts over and standardizes data to support both reference genomes [upl. by Nnylassej120]

MH Guide lifts over and standardizes data to support both reference genomes

Duration: 1:06
55 weergaven | 3 mrt. 2023

Finding Minor Allele Frequency MAF for SNP Genetic Variants from rsIDs or Position Info Using R [upl. by Fortier]

Finding Minor Allele Frequency MAF for SNP Genetic Variants from rsIDs or Position Info Using R

Duration: 38:23
3K weergaven | 8 sep. 2021

1 UCSC Genome Browser Tutorial the basics [upl. by Etselec]

1 UCSC Genome Browser Tutorial the basics

Duration: 8:41
93,1K weergaven | 5 sep. 2014

Molecular QC Interpreting your bioinformatics pipeline [upl. by Asehr]

Molecular QC Interpreting your bioinformatics pipeline

Duration: 36:53
423 weergaven | 29 jun. 2015

3 UCSC Genome Browser Tutorial BLAT [upl. by Nos]

3 UCSC Genome Browser Tutorial BLAT

Duration: 9:39
25,6K weergaven | 26 sep. 2014

13 Retrieving missense SNPs of a gene from gnomAD database for human genome assembly GRCh37hg19 [upl. by Matland]

13 Retrieving missense SNPs of a gene from gnomAD database for human genome assembly GRCh37hg19

Duration: 4:52
171 weergaven | 6 jan. 2022

12 Retrieving missense SNPs of a gene from ClinVar database for human genome assembly GRCh37hg19 [upl. by Isahella]

12 Retrieving missense SNPs of a gene from ClinVar database for human genome assembly GRCh37hg19

Duration: 4:39
115 weergaven | 9 maanden geleden

Demo 3 Old genome coordinates to new [upl. by Xylia]

Demo 3 Old genome coordinates to new

Duration: 2:44
1,7K weergaven | 11 okt. 2011

Deanna Church Dissecting the diagnostic yield of exome sequencing [upl. by Toback550]

Deanna Church Dissecting the diagnostic yield of exome sequencing

Duration: 59:14
303 weergaven | 19 mei 2015

511 Obtaining and filtering PROVEAN prediction result as well as adding custom SNP ID [upl. by Antonie]

511 Obtaining and filtering PROVEAN prediction result as well as adding custom SNP ID

Duration: 7:15
298 weergaven | 7 mrt. 2022

13 Retrieving missense SNPs of a gene from gnomAD database for human genome assembly GRCh37hg19 [upl. by Nyledaj498]

13 Retrieving missense SNPs of a gene from gnomAD database for human genome assembly GRCh37hg19

Duration: 4:49
14 weergaven | 2 maanden geleden

Liftover to Map Genomic Coordinates Between Genome Builds with Rtracklayer Bioconductor Package [upl. by Refinneg865]

Liftover to Map Genomic Coordinates Between Genome Builds with Rtracklayer Bioconductor Package

Duration: 1:06:41
1,4K weergaven | 19 okt. 2021

Rammstein Amerika Official Video [upl. by Campney]

Rammstein Amerika Official Video

Duration: 4:19
207,5mln. weergaven | 31 jul. 2015

mehter new york city [upl. by Nolyag]

mehter new york city

Duration: 2:26
2,9mln. weergaven | 21 mei 2012

How to align FASTQ files using BWA MEM [upl. by Brasca]

How to align FASTQ files using BWA MEM

Duration: 21:55
609 weergaven | 21 jul. 2022

Detection of mosaic and somatic structural variants with Sniffles2 [upl. by Maressa]

Detection of mosaic and somatic structural variants with Sniffles2

Duration: 10:50
23 weergaven | 1 maand geleden

Using population data to aid genomic data processing 基因體醫學月會 [upl. by Llerdna]

Using population data to aid genomic data processing 基因體醫學月會

Duration: 54:24
1,2K weergaven | 30 jun. 2021

Reference SNP IDs to Chromosome and Base Pair Genetic Variant Info with R Bioconductor [upl. by Ennairoc]

Reference SNP IDs to Chromosome and Base Pair Genetic Variant Info with R Bioconductor

Duration: 44:59
481 weergaven | 23 dec. 2021

Lucie Amerika [upl. by Laughton408]

Duration: 5:33
3,4mln. weergaven | 4 mrt. 2011

Predicting the Deleteriousness of Genomic Variants – Big and Small [upl. by Moina197]

Predicting the Deleteriousness of Genomic Variants – Big and Small

Duration: 2:31
12,3mln. weergaven | 21 mrt. 2011

Scarface In between us ft Nas [upl. by Notsgnik772]

Scarface In between us ft Nas

Duration: 26:55
347 weergaven | 12 jul. 2022

Identification of structural variation in chimpanzee using optical mapping and nanopore sequencing [upl. by Andie89]

Identification of structural variation in chimpanzee using optical mapping and nanopore sequencing

Duration: 5:03
2,6mln. weergaven | 26 nov. 2007

[upl. by Evonne]

Duration: 10:03
144 weergaven | 23 feb. 2021

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