Are there any tools capable of performing multi sequence alignment and tree construction that can handle up to 100,000 sequences?
Seqanswers Leaderboard Ad
Collapse
Announcement
Collapse
No announcement yet.
X
-
Originally posted by brachysclereid View PostAre there any tools capable of performing multi sequence alignment and tree construction that can handle up to 100,000 sequences?
In order to do what you are asking, you really should cluster the sequences first, then align from smaller sets.
MUSCLE's manual recommends using the UCLUST tool in USEARCH (http://www.drive5.com/usearch/) to reduce the number of alignments needed. And if you contact MUSCLE's author (http://www.drive5.com/muscle/about.htm) he mentions that he is working on something to leverage MUSCLE and USEARCH to deal with huge numbers of sequence alignments (without overly sacrificing accuracy).Michael Black, Ph.D.
ScitoVation LLC. RTP, N.C.
-
Are your sequences all from the same locus, e.g. amplicon sequenced? If so, the usual approach to build a phylogeny involves first taking a representative subset, say 500 sequences, and building a profile HMM using HMMer3 or building a SCFG using Infernal if the sequences are RNA with known secondary structure. With your HMM or SCFG in hand you can then quickly construct a multiple alignment of all 100k of them. see hmmalign. You can then feed the alignment to Morgan Price's FastTree or one of the other programs that can construct a phylogeny in subquadratic time.
That approach works well if you care only about substitutions in the evolutionary history (this is what most people want since they usually hold the richest evolutionary signal). If you care about indel histories you will have to do a full multiple sequence alignment with something like MUSCLE, MAFFT or another tool. I am not aware of any indel history inference tools that can operate on such large datasets. Maybe someone else knows of such methods?
Comment
-
building a cladogram with 100,000 sequences
Thanks for all the advice. It will take a while to sort through all the possibilities. Perhaps clustering first will be a good approach.
I'll make a post if I can get something to work. In the mean time other suggestions would be greatly appreciated!
Comment
Latest Articles
Collapse
-
by seqadmin
Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...-
Channel: Articles
12-16-2024, 07:57 AM -
-
by seqadmin
Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.
Long-Read Sequencing
Long-read sequencing has seen remarkable advancements,...-
Channel: Articles
12-02-2024, 01:49 PM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, 12-17-2024, 10:28 AM
|
0 responses
33 views
0 likes
|
Last Post
by seqadmin
12-17-2024, 10:28 AM
|
||
Started by seqadmin, 12-13-2024, 08:24 AM
|
0 responses
49 views
0 likes
|
Last Post
by seqadmin
12-13-2024, 08:24 AM
|
||
Started by seqadmin, 12-12-2024, 07:41 AM
|
0 responses
34 views
0 likes
|
Last Post
by seqadmin
12-12-2024, 07:41 AM
|
||
Started by seqadmin, 12-11-2024, 07:45 AM
|
0 responses
46 views
0 likes
|
Last Post
by seqadmin
12-11-2024, 07:45 AM
|
Comment