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Showing : SNPs • reset
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54
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bayenv2: "initial epsilon zero or 1 locus 6912"
6 months ago sonia.olaechea • 90 • updated 6 months ago katuckele • 10
0
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1
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4.7k
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Applying hard filters for variants
4.1 years ago bioinforesearchquestions • 230 • updated 6 months ago Biostar 20
0
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0
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67
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Suggest vcf filtered parameter for gatk VariantFiltration
6 months ago Mbillah • 110 • updated 6 months ago WouterDeCoster 39k
1
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3
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117
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In which step should plink be used?
6 months ago felipead66 • 30 • updated 6 months ago WouterDeCoster 39k
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2
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109
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Checking regions with high density of SNPs
7 months ago bwczech • 70
0
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2
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113
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Lots of alleles in the same place?
7 months ago tbb21 • 10 • updated 7 months ago Kevin Blighe 43k
2
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8
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179
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Merge two files depending on multiple matching columns
7 months ago iya837 • 0
1
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2
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167
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Summary from a vcf file
7 months ago felipead66 • 30 • updated 7 months ago arup ♦ 1.3k
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2
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122
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minimum snp number from set in LD
8 months ago RNAseqer • 110 • updated 8 months ago MatthewP • 110
3
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2
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149
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pulling snps from vcf file using ids
8 months ago RNAseqer • 110 • updated 8 months ago Kevin Blighe 43k
1
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0
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109
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Error in snphylo
8 months ago felipead66 • 30 • updated 8 months ago zx8754 7.5k
1
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1
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122
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query and export SNPs information from ensembl
8 months ago landivincenzo • 0 • updated 8 months ago Ben_Ensembl • 980
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12
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312
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SNps and calculation of sample size
9 months ago efsvdo • 0 • updated 9 months ago pltbiotech_tkarthi • 170
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187
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From mpileup on bam files to TMB calculation, how is it done?
9 months ago Pin.Bioinf • 240
1
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5
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345
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Difference between Private SNPs and Singleton SNPs
10 months ago prasundutta87 • 330
5
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8
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952
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VariantCalling with single sanger read
3.3 years ago Amirosein • 70 • updated 10 months ago trausch ♦ 1.3k
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202
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Change ALT field in VCF
10 months ago sonia.olaechea • 90
1
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8
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429
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How to calculate the fraction of bases that are different from the reference base using samtools mpileup ?
10 months ago M.O.L.S • 10
4
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5
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308
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PLINK assoc input: can it be two vcf files case/control?
11 months ago Pin.Bioinf • 240 • updated 11 months ago Kevin Blighe 43k
0
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1
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208
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Ensembl Biomart Allele Frequency for different ethnicity
11 months ago iside • 10
0
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2
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220
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Identifying consensus sequence between multiple Arabidopsis genome sequences
11 months ago bioinforesearchquestions • 230
3
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4
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1.2k
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Extract SNPs and SNP ID's from vcf file
2.1 years ago aadhirareddy1323 • 20 • updated 11 months ago zx8754 7.5k
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2
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1.6k
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GATK DP filter for multiple samples
3.4 years ago sun.nation • 120 • updated 12 months ago Flávia Rogério • 0
6
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6
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614
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1000Genomes population allele frequencies for list of SNPs
12 months ago sonia.olaechea • 90 • updated 12 months ago Pierre Lindenbaum 120k
17
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25
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20k
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7 follow
Remove columns and rows which have only NAs without deleting all the data
2.4 years ago ElenaL • 0 • updated 12 months ago slegotsky • 0
0
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2
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1.4k
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Hardy-Weinbergy Equilibrium and SNPs
4.1 years ago waynestatetutor • 0 • updated 12 months ago Biostar 20
2
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3
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1.1k
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Nanopore SNP and indels calling tool
16 months ago tarek.mohamed • 250 • updated 12 months ago WouterDeCoster 39k
0
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3
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293
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find LD of list of SNPs, located on different chromosomes
12 months ago anamaria • 40 • updated 12 months ago toralmanvar • 760
9
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3
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23k
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Obtaining The Snp Rs Number With The Chromosomal Position
6.6 years ago Sheila • 300 • updated 12 months ago hsiaoyi0504 • 40
10
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10
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771
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Minor allele frequency
3.0 years ago alessandrotestori7 • 330 • updated 13 months ago Biostar 20
3
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3
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467
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How to download VCF of 1000 genome project with population frequencies?
13 months ago bioinforesearchquestions • 230 • updated 13 months ago finswimmer 11k
5
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3
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977
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GWAS in Plink - phenotype file format
13 months ago SGMS • 60 • updated 13 months ago zx8754 7.5k
0
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5
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464
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Error: Snakemake skiped a rule
13 months ago c.clarido • 50 • updated 13 months ago rizoic • 190
0
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2
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338
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Best practices for variant calling on multiple sequencing runs of the same sample
14 months ago Damian Kao 15k • updated 14 months ago swbarnes2 5.7k
0
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0
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301
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GTEX - how to upload more than one rsIDs to get gene expression or eQTL information
14 months ago SGMS • 60
1
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1
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706
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Error: Line 2 of .ped file has more tokens than expected.
14 months ago sonia.olaechea • 90 • updated 14 months ago zx8754 7.5k
5
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9
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918
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7 follow
Need help with R script to edit x-axis of snp density plot
16 months ago deepti1rao • 20 • updated 14 months ago bernatgel ♦ 1.9k
6
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11
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419
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Finding out if certain SNP positions fall into certain gene regions
14 months ago SGMS • 60 • updated 14 months ago Alex Reynolds 28k
1
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3
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364
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Preference about IMPUTATION TOOL
15 months ago wonseok.cchoi • 0 • updated 14 months ago thassia.carratto • 10
1
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2
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267
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Using one bam file with huge coverage, How to generate several bam files with different coverage
15 months ago tarek.mohamed • 250 • updated 15 months ago WouterDeCoster 39k
213 results • Page 1 of 6
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Answer: test question 1
Answer: test question 1
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New test post with the AJAX system
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Markdown
A: Which Are The Best Programming Languages For A Bioinformatician?
A: Which Are The Best Programming Languages For A Bioinformatician?
Answer: Which Are The Best Programming Languages For A Bioinformatician?
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Recent Replies
Comment: " testing dfg " by Natay Aberra 0
Thanks a lot!
Comment: " testing dfg " by RamRS 21k
Drag and drop is frigging ***AWESOME***
Answer: " testing dfg " by Natay Aberra 0
Hello, test drag and drop of comments
Comment: " testing dfg " by RamRS 21k
Testing twitter embedding: https://www.twitter.com/statnews/status/656174802911129600 https://twitter.com/statnews/status/660506539762057…
Answer: test question 1 by Linda • 20
more than 10 characters
Comment: Which Are The Best Programming Languages For A Bioinformatician? by Digital • 0
https://www.digitalumbrellas.com/ Welcome to Digital Umbrella Pakistan, USA, UK. A Service company you can Depend on
Comment: " testing dfg " by RamRS 21k
Testing highlighting functionality. Using `<span style="background-color: #FFFF00">`: <span style="background-color: #FFFF00">Span trial</…
Comment: " testing dfg " by RamRS 21k
Testing <u>underline</u> functionality.
Comment: " testing dfg " by RamRS 21k
Testing comment with parentheses in URL: (this URL: https://www.ncbi.nlm.nih.gov/search/all/?term=BRCA1%20AND%20(Human%20OR%20Mouse))
Comment: get gene biotype for hg38 refseq by Natay Aberra 0
test the bumping
Comment: get gene biotype for hg38 refseq by genomax 68k
http://test.biostars.org/accounts/profile/2/ http://test.biostars.org/p/34/
Comment: New test post with the AJAX system by Natay Aberra 0
Yeah we will probably end up doing that.
Comment: Markdown by Natay Aberra 0
http://test.biostars.org/accounts/profile/18713/ http://test.biostars.org/p/p371267/#p371295 test the bumping
Comment: Markdown by Natay Aberra 0
http://test.biostars.org/p/p371285/ http://test.biostars.org/accounts/profile/user-2/
Comment: New test post with the AJAX system by genomax 68k
Checking to see if this comment bumps the thread to top.
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